C. Griscelli

发表

[Non-Hodgkin lymphoma arising in a case of Waldmann's intestinal lymphangiectasis].

P. Hérait, C. Gisselbrecht, C. Fermé, 1985, Nouvelle revue francaise d'hematologie.

Development of immunologic functions after bone marrow transplantation in 33 patients with severe combined immunodeficiency.

A. Fischer, C. Griscelli, F. Le Deist, 1989, Blood.

Infusion of Fcγ fragments for treatment of children with acute immune thrombocytopenic purpura

W. Fridman, C. Griscelli, P. Reinert, 1993, The Lancet.

Detection of HIV-specific cell-mediated cytotoxicity in the peripheral blood from infected children.

C. Griscelli, D. Schmitt, S. Blanche, 1993, Journal of immunology.

Inositol 1,4,5-trisphosphate- and arachidonic acid-induced calcium mobilization in T and B lymphocytes.

C. Griscelli, F. Le Deist, A. Fischer, 1990, Cellular immunology.

Lactoferrin deficiency as a consequence of a lack of specific granules in neutrophils from a patient with recurrent infections. Detection by immunoperoxidase staining for lactoferrin and cytochemical electron microscopy.

C. Griscelli, J. Vildé, D. Mason, 1980, The American journal of pathology.

Role of prostaglandin E2 in the induction of nonspecific T lymphocyte suppressor activity.

C. Griscelli, A. Durandy, A. Fischer, 1981, Journal of immunology.

Longitudinal study of 94 symptomatic infants with perinatally acquired human immunodeficiency virus infection. Evidence for a bimodal expression of clinical and biological symptoms.

F. Deist, C. Griscelli, C. Rouzioux, 1990, American journal of diseases of children.

Idiopathic disseminated bacillus Calmette-Guérin infection: a French national retrospective study.

C. Griscelli, J. Emile, J. Stéphan, 1996, Pediatrics.

A familial T‐cell lymphoma with γδ phenotype and an original location: Possible role of chronic Epstein–Barr virus infection

S. Schraub, C. Bodemer, F. Sigaux, 1996 .

Natural history of human immunodeficiency virus type 1 infection in children: prognostic value of laboratory tests on the bimodal progression of the disease.

A. Spira, C. Griscelli, A. Messiah, 1992, The Pediatric infectious disease journal.

A Prospective Study of Infants Born to Women Seropositive for Human Immunodeficiency Virus Type I

F. Deist, C. Griscelli, C. Rouzioux, 1990 .

Tracheomegaly and immune deficiency syndromes in childhood.

C. Griscelli, S. Chagnon, Y. Menu, 1981, Annales de radiologie.

Evaluation of D-penicillamine in juvenile chronic arthritis. A double-blind, multicenter study.

C. Griscelli, A. Prieur, P. Bordigoni, 1985, Arthritis and rheumatism.

Stroke and cerebral infarcts in children infected with human immunodeficiency virus.

G. Sebag, C. Griscelli, M. Tardieu, 1994, Archives of pediatrics & adolescent medicine.

DETECTION OF HTV1 DNA IN INFANTS AND CHILDREN BY MEANS OF THE POLYMERASE CHAIN REACTION

C. Griscelli, C. Rouzioux, C. Bréchot, 1988, The Lancet.

Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantation.

A. Fischer, C. Griscelli, M. Rolland, 1990, The New England journal of medicine.

An HLA-DRα promoter DNA-binding protein is expressed ubiquitously and maps to human chromosomes 22 and 5

R. Eddy, T. Shows, C. Griscelli, 2004, Immunogenetics.

Inherited immunodeficiency with a defect in a major histocompatibility complex class II promoter-binding protein differs in the chromatin structure of the HLA-DRA gene

P. Gönczy, W. Reith, B. Mach, 1989, Molecular and cellular biology.

Intractable infant diarrhea associated with phenotypic abnormalities and immunodeficiency.

A. Fischer, C. Griscelli, N. Brousse, 1994, The Journal of pediatrics.

Congenital and acquired lactoferrin deficiencies in neutrophils.

C. Griscelli, J. Vildé, J. Hakim, 1982, Advances in Experimental Medicine and Biology.

The gut‐associated lymphoid system: nature and properties of the large dividing cells

C. Griscelli, P. Vassalli, D. Guy‐grand, 1974, European journal of immunology.

Intraepithelial lymphocytes of human gut: isolation, characterisation and study of natural killer activity.

C. Griscelli, N. Cerf-Bensussan, D. Guy‐grand, 1985, Gut.

Peyer's patches, gut IgA plasma cells and thymic function: study in nude mice bearing thymic grafts.

C. Griscelli, P. Vassalli, D. Guy‐grand, 1975, Journal of immunology.

THE DISTRIBUTION OF LARGE DIVIDING LYMPH NODE CELLS IN SYNGENEIC RECIPIENT RATS AFTER INTRAVENOUS INJECTION

C. Griscelli, P. Vassalli, R. McCluskey, 1969, The Journal of experimental medicine.

Opposing effects of protein tyrosine kinase inhibitors on the monoclonal antibody induced internalization of CD3 and CD4 antigens

C. Griscelli, F. Selz, J. Pérignon, 1991, European journal of immunology.

The disappearance of germinal centers in chronic lymphadeno-hepato-splenomegaly syndrome in childhood: report of three cases.

C. Griscelli, C. Nezelof, C. Maupas, 1989, Pediatric pathology.

A trans-acting class II regulatory gene unlinked to the MHC controls expression of HLA class II genes

B. Mach, C. Griscelli, B. Lisowska‐Grospierre, 1985, Nature.

Natural killer and killer cell activities in patients with primary immunodeficiencies or defects in immune interferon production

M. Lipinski, C. Griscelli, T. Tursz, 1980, European journal of immunology.

Relation of the course of HIV infection in children to the severity of the disease in their mothers at delivery

C. Griscelli, C. Rouzioux, F. Monpoux, 1994, The New England journal of medicine.

The use of viral culture and p24 antigen testing to diagnose human immunodeficiency virus infection in neonates

C. Griscelli, C. Rouzioux, S. Blanche, 1992, The New England journal of medicine.

[Prognosis of the systemic forms of juvenile chronic arthritis. Apropos of 100 cases].

C. Griscelli, A. Prieur, C. Brémard-Oury, 1984, Archives francaises de pediatrie.

Common Variable Hypogammaglobulinemia in Children: Clinical and Immunologic Observations in 30 Patients

C. Griscelli, J. Virelizier, D. Buriot, 1983 .

Carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.

C. Griscelli, A. Durandy, F. Le Deist, 1992, American journal of medical genetics.

Rheumatoid rosette in juvenile rheumatoid arthritis

C. Griscelli, A. Prieur, J. Ballet, 1974, Archives of disease in childhood.

A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patients.

C. Griscelli, A. Prieur, D. Lovell, 1987, Scandinavian journal of rheumatology. Supplement.

SPECIFIC INTERLEUKIN-1 INHIBITOR IN SERUM AND URINE OF CHILDREN WITH SYSTEMIC JUVENILE CHRONIC ARTHRITIS

C. Griscelli, A. Prieur, J. Dayer, 1987, The Lancet.

Acute hemorrhagic, hepatic, and neurologic manifestations in juvenile rheumatoid arthritis: possible relationship to drugs or infection.

C. Griscelli, A. Prieur, M. Hadchouel, 1985, The Journal of pediatrics.

Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype

A. Fischer, S. Orkin, C. Griscelli, 1988, Human Genetics.

Arthropathy with rash, chronic meningitis, eye lesions, and mental retardation.

C. Griscelli, A. Prieur, 1981, The Journal of pediatrics.

Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A.

F. Ledeist, C. Griscelli, J. Stéphan, 1993, Blood.

Enhanced plasminogen-activator production by leukocytes in the human and murine Chediak-Higashi syndrome.

C. Griscelli, A. Durandy, G. de Saint Basile, 1985, Blood.

Impaired natural killer activity in lymphohistiocytosis syndrome.

C. Griscelli, F. Arenzana‐Seisdedos, J. Virelizier, 1984, The Journal of pediatrics.

Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A

F. Ledeist, C. Griscelli, J. Stéphan, 1993 .

Rapid Publication Atriopeptin III A Potent Natriuretic, Diuretic, and Hypotensive Agent in Rats with Chronic Renal Failure

C. Griscelli, A. Durandy, D. Charron, 2022 .

TREATMENT OF CENTRAL NERVOUS SYSTEM B LYMPHOPROLIFERATIVE SYNDROME BY LOCAL INFUSION OF A B CELL‐SPECIFIC MONOCLONAL ANTIBODY

A. Fischer, F. Deist, C. Griscelli, 1992, Transplantation.

cytological, immunological, and molecular characterization T-cell nonmalignant clonal proliferation in ataxia telangiectasia: a

P. Debré, A. Aurias, C. Griscelli, 2012 .

T-cell nonmalignant clonal proliferation in ataxia telangiectasia: a cytological, immunological, and molecular characterization.

P. Debré, A. Aurias, C. Griscelli, 1989, Blood.

Role of the LFA-1 molecule in cellular interactions required for antibody production in humans.

A. Fischer, C. Griscelli, A. Durandy, 1986, Journal of immunology.

Impaired defense against vaccinia in a child with T-lymphocyte deficiency associated with inosine phosphorylase defect.

C. Griscelli, J. Ballet, P. Reinert, 1978, The Journal of pediatrics.

Selective defect of precursor T cells associated with apparently normal B lymphocytes in severe combined immunodeficiency disease.

C. Griscelli, A. Durandy, J. Ballet, 1978, The Journal of pediatrics.

antithymocyte globulins, steroids, and cyclosporin A Treatment of familial hemophagocytic lymphohistiocytosis with

F. Ledeist, C. Griscelli, J. Stéphan, 2011 .

Improvements in methods for identifying patients with severe combined immunodeficiency and related syndromes.

C. Griscelli, A. Webster, L. Businco, 1977, Zeitschrift fur Immunitatsforschung. Immunobiology.

Defective monocyte functions in a child with fatal disseminated BCG infection.

A. Fischer, C. Griscelli, A. Durandy, 1980, Clinical immunology and immunopathology.

A syndrome associating partial albinism and immunodeficiency.

C. Griscelli, A. Durandy, D. Guy‐grand, 1978, The American journal of medicine.

Molecular characterization of different ataxia telangiectasia T-cell clones

G. Thomas, A. Aurias, M. Stern, 2004, Human Genetics.

Restriction of the in vitro anti-mannan antibody response by HLA-DQ molecules.

C. Griscelli, A. Durandy, D. Charron, 1986, Human immunology.

Specific protease deficiency in polymorphonuclear leukocytes of Chediak- Higashi syndrome and beige mice

C. Griscelli, J. Vassalli, A. Granelli‐Piperno, 1978, The Journal of experimental medicine.

Specific binding of antigen onto human T lymphocytes.

C. Griscelli, A. Durandy, D. Charron, 1986, The Journal of clinical investigation.

N-ISOPROPYL-ALPHA-(2-METHYLHYDRAZINO)-P-TOLUAMIDE, HYDROCHLORIDE (NSC-77213) IN TREATMENT OF SOLID TUMORS.

C. Griscelli, J. Schlumberger, G. Brulé, 1965, Cancer chemotherapy reports.

PERSISTENT EPSTEIN-BARR VIRUS INFECTION IN A CHILD WITH HYPERGAMMAGLOBULINÆMIA AND IMMUNOBLASTIC PROLIFERATION ASSOCIATED WITH A SELECTIVE DEFECT IN IMMUNE INTERFERON SECRETION

C. Griscelli, G. Lenoir, J. Virelizier, 1978, The Lancet.

Cell Membrane Abnormalities Leading to Immune Deficiency

C. Griscelli, 1986 .

Combined immunodeficiency with defective expression in major histocompatibility complex class II genes.

C. Griscelli, 1991, Clinical immunology and immunopathology.

Combined immunodeficiency with abnormal expression of MHC class II genes.

B. Mach, C. Griscelli, A. Durandy, 1989, Clinical immunology and immunopathology.

Defect of Expression of MHC Genes Responsible for an Abnormal HLA Class I Phenotype and the Class II Negative Phenotype of Lymphocytes from Patients with Combined Immunodeficiency

B. Mach, C. Griscelli, A. Durandy, 1984 .

Biotin-responsive immunoregulatory dysfunction in multiple carboxylase deficiency

A. Munnich, C. Griscelli, J. Frézal, 1981, Journal of Inherited Metabolic Disease.

Biotin-responsive immunoregulatory dysfunction in multiple carboxylase deficiency

A. Munnich, C. Griscelli, J. Frézal, 2004, Journal of Clinical Immunology.

Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodies.

C. Griscelli, M. Lebret, F. Rendu, 1983, The American journal of pathology.

Successful HLA nonidentical bone marrow transplantation in three patients with the leukocyte adhesion deficiency.

A. Fischer, V. Wahn, C. Griscelli, 1989, Blood.

The effects of indomethacin administration during pregnancy on women's and newborns' T-suppressor lymphocyte activity and on HLA class II expression by newborns' leukocytes.

C. Griscelli, A. Durandy, C. Brami, 1985, American journal of reproductive immunology and microbiology : AJRIM.

BONE-MARROW TRANSPLANTATION FOR IMMUNODEFICIENCIES AND OSTEOPETROSIS: EUROPEAN SURVEY, 1968-1985

A. Fischer, G. Morgan, W. Friedrich, 1986, The Lancet.

Immunoglobulins in ataxia-telangiectasia: evidence for IgG4 and IgA2 subclass deficiencies.

C. Griscelli, C. Rivat, J. Salier, 1981, Clinical immunology and immunopathology.

Timing of mother‐to‐child HIV‐1 transmission depends on maternal status

A. Valleron, C. Griscelli, C. Rouzioux, 1993, AIDS.

Prevention of graft failure by an anti human leukocyte functional antigen 1 monoclonal antibody in hla mismatched bone marrow transplantation

A. Fischer, D. Olive, C. Griscelli, 1986 .

PREVENTION OF GRAFT FAILURE BY AN ANTI-HLFA-1 MONOCLONAL ANTIBODY IN HLA-MISMATCHED BONE-MARROW TRANSPLANTATION

A. Fischer, F. Deist, D. Olive, 1986, The Lancet.

Primary membrane T cell immunodeficiencies.

C. Griscelli, G. de Saint Basile, N. Cerf-Bensussan, 1991, Clinical immunology and immunopathology.

Mannan-specific and mannan-induced T-cell suppressive activity in patients with chronic mucocutaneous candidiasis

C. Griscelli, A. Durandy, A. Fischer, 1987, Journal of Clinical Immunology.

Reduction of graft failure by a monoclonal antibody (anti-LFA-1 CD11a) after HLA nonidentical bone marrow transplantation in children with immunodeficiencies, osteopetrosis, and Fanconi's anemia: a European Group for Immunodeficiency/European Group for Bone Marrow Transplantation report.

A. Fischer, W. Friedrich, C. Griscelli, 1991, Blood.

Immunogenicity ofHaemophilus influenzae type b capsular polysaccharide and its tetanus toxoid conjugate in patients with recurrent infections or humoral immunodeficiency

C. Griscelli, J. Preud’homme, B. Fritzell, 1992, International journal of clinical & laboratory research.

Prenatal diagnosis of syndromes associating albinism and immune deficiencies (Chediak‐Higashi syndrome and variant)

C. Griscelli, A. Durandy, D. Guy‐grand, 1993, Prenatal diagnosis.

Immunoelectron‐microscopic Localization of Immunoglobulin A and Secretory Component in Jejunal Mucosa from Children with Coeliac Disease

C. Griscelli, J. Jos, F. Labbé, 1979, Scandinavian journal of immunology.

Immunoglobulins on the surface of lymphocytes in fifty patients with primary immunodeficiency diseases.

C. Griscelli, J. Preud’homme, M. Seligmann, 1973, Clinical immunology and immunopathology.

T‐Cell Subset Analysis by Monoclonal Antibodies in Primary Immunodeficiences

C. Griscelli, A. Durandy, F. Phan-Dinh-Tuy, 1981, Scandinavian journal of immunology.

Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural course.

A. Fischer, C. Griscelli, J. Hermans, 1994, Pediatrics.

Long-term itraconazole prophylaxis against Aspergillus infections in thirty-two patients with chronic granulomatous disease.

A. Fischer, C. Griscelli, J. Levron, 1994, The Journal of pediatrics.

Hyper-IgM immunodeficiency syndrome: Influence of lymphokines onin vitro maturation of peripheral B cells

A. Fischer, C. Griscelli, J. Thèze, 1992, Journal of Clinical Immunology.

Serum IgG subclass deficiency in ataxia-telangiectasia.

C. Griscelli, P. Aucouturier, J. Preud’homme, 1987, Clinical and experimental immunology.

Serum IgG subclass levels in patients with primary immunodeficiency syndromes or abnormal susceptibility to infections.

C. Griscelli, Y. Lebranchu, P. Aucouturier, 1989, Clinical immunology and immunopathology.

Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome.

A. Fischer, C. Klein, F. Ledeist, 1993, The Journal of pediatrics.

A study of 25 patients with chronic granulomatous disease: A new classification by correlating respiratory burst, cytochrome b, and flavoprotein

A. Fischer, C. Griscelli, R. Seger, 1986, Journal of Clinical Immunology.

Enzymatic deficiency in monocytes from patients with chronic granulomatous disease.

C. Griscelli, M. Gougerot-Pocidalo, J. Hakim, 1982, Advances in experimental medicine and biology.

Monocyte α‐naphtyl esterase deficiency in chronic granulomatous disease

C. Griscelli, M. Gougerot-Pocidalo, J. Hakim, 1981 .

Specific inhibition of in vitro Candida-induced lymphocyte proliferation by polysaccharidic antigens present in the serum of patients with chronic mucocutaneous candidiasis.

C. Griscelli, J. Ballet, A. Fischer, 1978, The Journal of clinical investigation.

Mannan Antigen of Candida Albicans and Cellular Immune Responses in Vitro and in Vivo

A. Fischer, C. Griscelli, A. Durandy, 1988 .

Prenatal testing for inherited immune deficiencies by fetal blood sampling

C. Griscelli, A. Durandy, R. Henrion, 1982, Prenatal diagnosis.

Severe combined immunodeficiency with B lymphocytes: a selective defect of precursor T cells

C. Griscelli, A. Durandy, F. Daguillard, 1979 .

Lymphotoxin (LT) production by lymphocytes from children with primary immunedeficiency disease.

C. Griscelli, A. Prieur, F. Daguillard, 1978, Clinical immunology and immunopathology.

Electrophoretic characteristics and membrane receptors of lymphocytes in primary immunodeficiency diseases.

C. Griscelli, A. Durandy, M. Wioland, 1975, Clinical immunology and immunopathology.

Dysfunctions of pokeweed mitogen-stimulated T and B lymphocyte responses induced by gammaglobulin therapy.

C. Griscelli, A. Durandy, A. Fischer, 1981, The Journal of clinical investigation.

Severe combined immunodeficiency with quantitatively normal but abnormally differentiated T lymphocytes.

E. Reinherz, C. Griscelli, A. Durandy, 1981, The Journal of pediatrics.

Enhancement by interferon of membrane HLA antigens in patients with combined immunodeficiency with defective HLA expression.

C. Griscelli, A. Durandy, J. Virelizier, 1983, Clinical and experimental immunology.

Nonspecific Alpha-Naphtyl Acetate Esterase Activity of T-Lymphocytes: Study in Healthy Newborns and Children, in Immune Deficiencies and Juvenile Rheumatoid Arthritis

C. Griscelli, A. Prieur, N. Wada, 1981, Pediatric Research.

Intraepithelial lymphocytes ofhumangut:isolation, characterisation andstudy ofnatural killer activity

C. Griscelli, N. Cerf-Bensussan, D. Guy‐grand, 2011 .

Respective Roles and Interactions of T Lymphocyte and PGE2‐Mediated Monocyte Suppressive Activities in Human Newborns and Mothers at the Time of Delivery

C. Griscelli, A. Durandy, S. Mamas, 1982, American journal of reproductive immunology : AJRI : official journal of the American Society for the Immunology of Reproduction and the International Coordination Committee for Immunology of Reproduction.

Letter: HL-A antigens and immune deficiency states.

J. Dausset, C. Griscelli, J. Hors, 1974, British medical journal.

A second case of inosine phosphorylase deficiency with severe T-cell abnormalities.

C. Griscelli, C. De Bruyn, M. Hamet, 1977, Advances in experimental medicine and biology.

Incidence, severity, and prevention of infections in chronic granulomatous disease.

A. Fischer, C. Griscelli, R. Seger, 1989, The Journal of pediatrics.

The Role of PGE2 in the Induction of Suppressor Cells in Humans

F. Deist, C. Griscelli, A. Durandy, 1985 .

Activation of genetically major histocompatibility complex (MHC) class II-deficient B lymphocytes

C. Griscelli, M. Forveille, A. Durandy, 1989, Journal of Clinical Immunology.

FULMINANT MENINGOCOCCEMIA IN A CHILD WITH HEREDITARY DEFICIENCY OF THE SEVENTH COMPONENT OF COMPLEMENT AND PROTEINURIA

C. Griscelli, P. Berche, C. Loirat, 1980, Acta paediatrica Scandinavica.

[Cutaneous manifestations disclosing T-cell gamma/delta lymphoma in a 13-year-old-girl].

C. Bodemer, P. Agache, C. Griscelli, 1993, Annales de dermatologie et de venereologie.

Specific in vitro antimannan-rich antigen of Candida albicans antibody production by sensitized human blood lymphocytes.

C. Griscelli, A. Durandy, A. Fischer, 1983, The Journal of clinical investigation.

Neutrophil chemotaxis in juvenile chronic arthritis.

C. Griscelli, A. Prieur, P. Trung, 1980, Annals of the rheumatic diseases.

[Adenomegalic cytophagic sinusal histiocytosis. Morphological and immunologic study of a case].

C. Griscelli, F. Jaubert, R. Girot, 1978, Archives francaises de pediatrie.

Treatment of severe Epstein-Barr virus-induced polyclonal B-lymphocyte proliferation by anti-B-cell monoclonal antibodies. Two cases after HLA-mismatched bone marrow transplantation.

C. Griscelli, G. Lenoir, S. Blanche, 1988, Annals of internal medicine.

Early impairment of gut mucosal immunity in HIV‐1‐infected children

C. Griscelli, S. Blanche, P. Moja, 1994, Clinical and experimental immunology.

Two complementation groups account for most cases of inherited MHC class II deficiency.

M. Rols, C. Griscelli, A. Fischer, 1994, Human molecular genetics.

SPECIFIC ELIMINATION OF ALLOREACTIVE T CELLS BY AN ANTI‐INTERLEUKIN-2 RECEPTOR B CHAIN‐SPECIFIC IMMUNOTOXIN

A. Fischer, F. Deist, C. Griscelli, 1990, Transplantation.

RIBAVIRIN IN HTLV-III:LAV INFECTION OF INFANTS

A. Fischer, F. Deist, C. Griscelli, 1986, The Lancet.

ISOLATION OF NEW LYMPHOTROPIC RETROVIRUS FROM TWO SIBLINGS WITH HAEMOPHILIA B, ONE WITH AIDS

A. Fischer, C. Griscelli, J. Chermann, 1984, The Lancet.

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene

A. Fischer, C. Griscelli, O. Sanal, 1997, Nature Genetics.

Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).

A. Fischer, C. Griscelli, N. Brousse, 1991, The Journal of clinical investigation.

Transfer factor therapy in immuno-deficiencies.

C. Griscelli, J. Revillard, H. Bétuel, 1973, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

Endothelial Intracisternal Tubular Inclusions in a Case of Chronic Encephalitis Associated with Immunological Deficiency

C. Griscelli, P. Lebon, G. Lyon, 1972 .

Congenital toxoplasmosis. Fetal synthesis of oligoclonal immunoglobulin G in intrauterine infection.

C. Griscelli, G. Desmonts, D. Frommel, 1973, The Journal of pediatrics.

Primary immunodeficiency diseases: Report of a World Health Organization Scientific Group

T. Waldmann, C. Griscelli, F. Rosen, 1986 .

Treatment of Omenn syndrome by bone marrow transplantation.

A. Fischer, C. Griscelli, M. Cavazzana‐Calvo, 1995, The Journal of pediatrics.

Graft vs graft reaction resulting in the elimination of maternal cells in a SCID patient with maternofetal GVHd after an HLA identical bone marrow transplantation.

A. Fischer, C. Griscelli, F. Le Deist, 1987, Journal of immunology.

Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients.

A. Fischer, C. Griscelli, A. Durandy, 1993, The Journal of pediatrics.

Combined immunodeficiency with defective expression in MHC class II genes.

B. Mach, C. Griscelli, B. Lisowska‐Grospierre, 1989, Immunodeficiency reviews.

Rapid A Defect in the Regulation of Major Histocompatibility Complex Class 11 Gene Expression in Human HLA-DR Negative Lymphocytes from Patients with Combined Immunodeficiency Syndrome

B. Mach, C. Griscelli, A. Durandy, 2022 .

Partial albinism with immunodeficiency (Griscelli syndrome).

C. Klein, C. Griscelli, A. Durandy, 1994, The Journal of pediatrics.

Defective handling of mannan by monocytes in patients with chronic mucocutaneous candidiasis resulting in a specific cellular unresponsiveness.

C. Griscelli, A. Fischer, M. Audinot, 1982, Clinical and experimental immunology.

Selective tropism of lymphadenopathy associated virus (LAV) for helper-inducer T lymphocytes.

C. Griscelli, J. Chermann, F. Barré-Sinoussi, 1984, Science.

The mouse gut T lymphocyte, a novel type of T cell. Nature, origin, and traffic in mice in normal and graft-versus-host conditions

C. Griscelli, P. Vassalli, D. Guy‐grand, 1978, The Journal of experimental medicine.

Mother-child transmission of HIV-1 and infant survival in Brazzaville, Congo.

C. Griscelli, M. Sinet, S. Blanche, 1989, AIDS.

Antigen recognition by T lymphocytes. V. Life span of mouse spontaneous rosette-forming cells.

C. Griscelli, J. Bach, D. Guy‐grand, 1974, Cellular immunology.

New data on clonal anomalies of chromosome 14 in ataxia telangiectasia: tct (14;14) and inv(14)

B. Dutrillaux, A. Aurias, C. Griscelli, 2004, Human Genetics.

Estimated timing of mother-to-child human immunodeficiency virus type 1 (HIV-1) transmission by use of a Markov model. The HIV Infection in Newborns French Collaborative Study Group.

A. Valleron, C. Griscelli, C. Rouzioux, 1995, American journal of epidemiology.

Cellular immune deficiency in two siblings with hereditary orotic aciduria.

C. Griscelli, A. Durandy, R. Girot, 1983, The New England journal of medicine.

Megaloblastic Anemia and Immune Abnormalities in a Patient with Methionine Synthase Deficiency

C. Griscelli, J. Zittoun, J. Marquet, 1987, Acta paediatrica Scandinavica.

Early prenatal diagnosis of inherited severe immunodeficiencies linked to enzyme deficiencies.

C. Griscelli, A. Durandy, F. Freycon, 1987, The Journal of pediatrics.

A new ultramicrochemical assay for purine nucleoside phosphorylase.

C. Griscelli, C. De Bruyn, T. Oei, 1978, Analytical biochemistry.

Cytidine deaminase deficiency in a child with combined immunodeficiency: more than a coincidence?

A. Fischer, C. Griscelli, F. Arenzana‐Seisdedos, 1986, Advances in experimental medicine and biology.

Growth and growth hormone secretion after bone marrow transplantation.

A. Fischer, C. Griscelli, J. Souberbielle, 1993, Archives of disease in childhood.

A prospective study of infants born to women seropositive for human immunodeficiency virus type 1

C. Griscelli, C. Rouzioux, S. Blanche, 1990, The New England journal of medicine.

Anti-B-cell monoclonal antibodies in the treatment of severe B-cell lymphoproliferative syndrome following bone marrow and organ transplantation.

A. Fischer, C. Griscelli, P. Niaudet, 1991, The New England journal of medicine.

Gut-associated lymphoblasts and intestinal IgA plasma cells.

C. Griscelli, P. Vassalli, D. Guy‐grand, 1974, Advances in experimental medicine and biology.

ANTIMONIOTUNGSTATE (HPA 23) TREATMENT OF THREE PATIENTS WITH AIDS AND ONE WITH PRODROME

C. Griscelli, J. Chermann, F. Barré-Sinoussi, 1985, The Lancet.

Thymic abnormalities in fetuses aborted from human immunodeficiency virus type 1 seropositive women.

C. Griscelli, J. Roume, C. Bréchot, 1992, Pediatrics.

Cytotoxic T lymphocyte responses in the peripheral blood of children born to human immunodeficiency virus‐1‐infected mothers

C. Griscelli, R. Cheynier, S. Wain-Hobson, 1992, European journal of immunology.

Polymerase chain reaction for studies of mother to child transmission of HIV1 in Africa

C. Griscelli, C. Bréchot, M. Lallemant, 1990, Journal of medical virology.

Cancer risk in heterozygotes for ataxia‐telangiectasia

A. Aurias, C. Griscelli, D. Stoppa-Lyonnet, 2001, International journal of cancer.

Reversal of natural killer defect in a patient with Chédiak-Higashi syndrome after bone-marrow transplantation.

C. Griscelli, A. Durandy, P. Reinert, 1982, The New England journal of medicine.

Self‐tolerance to host and donor following HLA‐mismatched bone marrow transplantation

C. Griscelli, J. de Villartay, Alain Fischer, 1986, European journal of immunology.

A monoclonal antibody (HML‐1) defining a novel membrane molecule present on human intestinal lymphocytes

C. Griscelli, N. Brousse, A. Jarry, 1987, European journal of immunology.

Treatment of hemophagocytic lymphohistiocytosis with chemotherapy and bone marrow transplantation: a single-center study of 22 cases.

C. Griscelli, S. Blanche, J. Landman, 1991, Blood.

Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA)

M. Pembrey, A. Fischer, J. Goodship, 1987, Human Genetics.

Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families

A. Aurias, C. Griscelli, D. Stoppa-Lyonnet, 1999, British Journal of Cancer.

Detection of HIV1 DNA in infants and children by means of the polymerase chain reaction.

C. Griscelli, C. Rouzioux, C. Bréchot, 1988, Lancet.

Longitudinal study of 18 children with perinatal LAV/HTLV III infection: attempt at prognostic evaluation.

C. Griscelli, S. Chamaret, L. Montagnier, 1986, The Journal of pediatrics.

Antiimmunoglobulin Antibodies in Immunodeficiencies: Their Influence on Intolerance Reactions to γ‐globulin Administration

C. Griscelli, L. Caldera, J. Homberg, 1974 .

Alternative pathways for the development of lymphoid structures in humans

A. Fischer, C. Picard, N. Boddaert, 2021, Proceedings of the National Academy of Sciences.

Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.

A. Fischer, C. Griscelli, S. Malcolm, 1987, Proceedings of the National Academy of Sciences of the United States of America.

BONE-MARROW TRANSPLANTATION FOR INBORN ERROR OF PHAGOCYTIC CELLS ASSOCIATED WITH DEFECTIVE ADHERENCE, CHEMOTAXIS, AND OXIDATIVE RESPONSE DURING OPSONISED PARTICLE PHAGOCYTOSIS

A. Fischer, C. Griscelli, A. Durandy, 1983, The Lancet.

Allogeneic bone marrow transplantation for erythrophagocytic lymphohistiocytosis.

G. Leverger, C. Griscelli, A. Durandy, 1986, The Journal of pediatrics.

Treatment of four patients with erythrophagocytic lymphohistiocytosis by a combination of epipodophyllotoxin, steroids, intrathecal methotrexate, and cranial irradiation.

A. Fischer, C. Griscelli, F. Arenzana‐Seisdedos, 1985, Pediatrics.

Anti-immunoglobulin antibodies in immunodeficiencies: their influence on intolerance reactions to gamma-globulin administration.

C. Griscelli, L. Caldera, J. Homberg, 1974, Vox sanguinis.

genes rearrangement between T-cell receptor beta and T-cell receptor gamma Inversion of chromosome 7 in ataxia telangiectasia is generated by a

G. Thomas, A. Aurias, M. Stern, 2011 .

Inversion of chromosome 7 in ataxia telangiectasia is generated by a rearrangement between T-cell receptor beta and T-cell receptor gamma genes.

G. Thomas, A. Aurias, M. Stern, 1989, Blood.

Bone marrow transplantation in 26 patients with Wiskott-Aldrich syndrome from a single center.

A. Fischer, F. Deist, C. Griscelli, 1996, The Journal of pediatrics.

Immune response to Toxoplasma gondii in man. I. Common idiotypic determinants of toxoplasma-specific human antibodies.

C. Griscelli, B. Lisowska‐Grospierre, G. de Saint-Basile, 1981, Annales d'immunologie.

Severe combined immunodeficiencies

A. Fischer, C. Griscelli, 1990 .

European experience of bone-marrow transplantation for severe combined immunodeficiency

A. Fischer, G. Morgan, W. Friedrich, 1990, The Lancet.

Treatment of familial lymphohistiocytosis: chemotherapy or bone marrow transplant?

C. Griscelli, S. Blanche, A. Fischer, 1989, Pediatric hematology and oncology.

PIGMENT DILUTION AND IMMUNODEFICIENCY: A NEW SYNDROME

C. Griscelli, M. Prunieras, 1978, International journal of dermatology.

Prenatal diagnosis of severe combined immunodeficiency with defective synthesis of HLA molecules

C. Griscelli, A. Durandy, N. Cerf-Bensussan, 1987, Prenatal diagnosis.

Prenatal diagnosis of severe combined immunodeficiency.

C. Griscelli, A. Durandy, R. Henrion, 1982, The Journal of pediatrics.

ANTENATAL DIAGNOSIS OF SEVERE COMBINED IMMUNODEFICIENCY FROM FETAL CORD BLOOD

C. Griscelli, A. Durandy, J. Frézal, 1982, The Lancet.

Identification of the defective NADPH‐oxidase component in Chronic Granulomatous Disease: a study of 57 European families

A. Fischer, C. Griscelli, A. Segal, 1992, European journal of clinical investigation.

Interferon gamma for chronic granulomatous disease.

A. Fischer, C. Griscelli, J. Bourquin, 1991, The New England journal of medicine.

HLA-haploidentical bone marrow transplantation for severe combined immunodeficiency using E rosette fractionation and cyclosporine.

C. Griscelli, A. Durandy, F. Le Deist, 1986, Blood.

class II deficiency: a single-center study of 19 patients Bone marrow transplantation in major histocompatibility complex

A. Fischer, C. Klein, C. Griscelli, 2010 .

Hypoglycaemia induced by antibodies to insulin receptor following a bone marrow transplantation in an immunodeficient child

A. Fischer, C. Griscelli, E. Obberghen, 1989, Diabetologia.

Bone marrow transplantation in major histocompatibility complex class II deficiency: a single-center study of 19 patients.

A. Fischer, C. Klein, C. Griscelli, 1995, Blood.

Cost of allogeneic bone marrow transplantation in four diseases.

D. Jolly, C. Griscelli, C. Viens-Bitker, 1989, Health policy.

Treatment of Chediak-Higashi syndrome by allogenic bone marrow transplantation: report of 10 cases.

A. Fischer, E. Haddad, C. Griscelli, 1995, Blood.

[The accelerated phase of Chediak-Higashi syndrome].

C. Griscelli, C. Gaud, S. Blanche, 1989, Archives francaises de pediatrie.

Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.

A. Fischer, C. Griscelli, J. Mandel, 1990, American journal of human genetics.

[Chediak-Higashi disease: a new case treated by bone marrow allograft].

C. Griscelli, A. Fischer, A. Decoster, 1989, Annales de pediatrie.

LITHIUM THERAPY IN CONGENITAL NEUTROPENIA

C. Griscelli, A. Barrett, A. Faille, 1977, The Lancet.

X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers

A. Fischer, C. Griscelli, T. Lecompte, 1991, Annals of Hematology.

Impaired T8 lymphocyte-mediated suppressive activity in patients with partial Di George syndrome

F. Deist, C. Griscelli, A. Durandy, 1986, Journal of Clinical Immunology.

Molecular and functional anomalies in two new mutant glucose-phosphate-isomerase variants with enzyme deficiency and chronic hemolysis

C. Griscelli, A. Kahn, R. Girot, 1978, Human Genetics.

Deficiency of the adhesive protein complex lymphocyte function antigen 1, complement receptor type 3, glycoprotein p150,95 in a girl with recurrent bacterial infections. Effects on phagocytic cells and lymphocyte functions.

C. Griscelli, A. Durandy, M. Kazatchkine, 1985, The Journal of clinical investigation.

Genotyping with DNA probes in combined immunodeficiency syndrome with defective expression of HLA.

J. Dausset, D. Cohen, C. Griscelli, 1985, The New England journal of medicine.

Human severe combined immunodeficiency disease: phenotypic and functional characteristics of peripheral B lymphocytes.

C. Griscelli, J. Thèze, F. Le Deist, 1990, Journal of immunology.

[Hypoplasia of cartilage and hair with combined immune deficiency].

A. Fischer, C. Griscelli, F. Le Deist, 1989, Annales de pediatrie.

Severe combined immunodeficiency disease: a pathological analysis of 26 cases.

C. Griscelli, S. Gosseye, C. Nezelof, 1983, Clinical immunology and immunopathology.

Granulopoietic differentiation in long‐term bone marrow cultures from children with congenital neutropenia

C. Griscelli, L. Coulombel, C. Parmentier, 1988, American journal of hematology.

Epstein-Barr virus-associated hemophagocytic syndrome: clinical presentation and treatment.

C. Griscelli, S. Blanche, A. Fischer, 1989, Pediatric hematology and oncology.

BONE-MARROW TRANSPLANTATION IN OSTEOPETROSIS

C. Griscelli, J. Ballet, J. Reeves, 1977, The Lancet.

[The Wiskott-Aldrich syndrome].

C. Griscelli, B. Belohradsky, W. Marget, 2020, Ergebnisse der inneren Medizin und Kinderheilkunde.

B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?

A. Fischer, A. Munnich, C. Griscelli, 2001, Journal of medical genetics.

Effects of interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α) on the expression of LFA-1 in the moderate phenotype of leukocyte adhesion deficiency (LAD)

M. Dimanche-Boitrel, C. Griscelli, A. Fischer, 1989, Journal of Clinical Immunology.

Clinical consequences and treatment of primary immunodeficiency syndromes characterized by functional T and B lymphocyte anomalies (combined immune deficiency).

A. Fischer, C. Griscelli, F. Le Deist, 1994, Pediatrics.

Genetic study of a new X-linked recessive immunodeficiency syndrome.

A. Fischer, C. Griscelli, Y. Lebranchu, 1992, The Journal of clinical investigation.

Structural analysis of low TCR-CD3 complex expression in T cells of an immunodeficient patient.

C. Griscelli, F. Le Deist, A. Fischer, 1992, The Journal of biological chemistry.

[Precocious histiocytosis X with cutaneous nodules. Favorable evolution].

C. Griscelli, L. Boniface, D. Buriot, 1978, Annales de dermatologie et de venereologie.

Transplantation of Lymphoid Cells in Patients with Severe Combined Immunodeficiency (SCID)

C. Griscelli, A. Durandy, D. Buriot, 1980 .

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β

A. Fischer, L. Notarangelo, C. Griscelli, 1992, Human Genetics.

Analysis of the membrane glycoproteins of platelets in the Wiskott‐Aldrich syndrome

F. Deist, C. Griscelli, A. Durandy, 1988, British journal of haematology.

Congenital immunodeficiency with a regulatory defect in MHC class II gene expression lacks a specific HLA-DR promoter binding protein, RF-X

W. Reith, B. Mach, C. Griscelli, 1988, Cell.

Zidovudine therapy in children with acquired immunodeficiency syndrome.

C. Griscelli, C. Rouzioux, G. Duhamel, 1988, The American journal of medicine.

Infusion of Fc gamma fragments for treatment of children with acute immune thrombocytopenic purpura.

W. Fridman, C. Griscelli, P. Reinert, 1993, Lancet.

[HIV infection in infants].

C. Griscelli, 1987, Pediatrie.

POSSIBLE TRANSMISSION OF A HUMAN LYMPHOTROPIC RETROVIRUS (LAV) FROM MOTHER TO INFANT WITH AIDS

A. Fischer, V. Vié, F. Brun-Vézinet, 1984, The Lancet.

BONE-MARROW TRANSPLANTATION IN OSTEOPETROSIS

C. Griscelli, J. Ballet, G. Milhaud, 1977, The Lancet.

Tandem translocation t(14;14) in isolated and clonal cells in ataxia telangiectasia are different

B. Dutrillaux, A. Aurias, C. Griscelli, 2004, Human Genetics.

Separation of precursor T cells and Ig-secreting B cells from the large lymphocytic cells of human tonsil.

C. Griscelli, A. Durandy, J. Ballet, 1977, Cellular immunology.

LFA‐1 β‐chain synthesis and degradation in patients with leukocyte‐adhesive proteins deficiency

C. Griscelli, M. Arnaout, A. Fischer, 1987, European journal of immunology.

Leukocyte Adhesion Deficiency as a Model for the Study of the Functional Role of LFA-1

M. Dimanche-Boitrel, C. Griscelli, A. Fischer, 1990 .

In vivo infusion of anti LFA-1 antibody in HLA non-identical bone marrow transplantation in children: serum concentrations and biological effects.

A. Fischer, C. Griscelli, L. Chatenoud, 1989, Bone marrow transplantation.

Intestinal, Salivary, and Tonsillar IgA and J‐Chain Production in a Patient with Severe Deficiency of Serum IgA

C. Griscelli, P. Brandtzaeg, D. Guy‐grand, 1981, Scandinavian journal of immunology.

A familial occurrence of natural killer cell‐T‐lymphocyte proliferation disease in two children

C. Griscelli, G. de Saint Basile, L. Coulombel, 1991, Cancer.

NF-X, a transcription factor implicated in MHC class II gene regulation.

V. Kouskoff, C. Benoist, C. Griscelli, 1991, Journal of immunology.

Bone marrow transplantation in a patient with Chédiak-Higashi Syndrome.

C. Griscelli, J. Virelizier, 1983, Birth defects original article series.

Possible toxicity of levamisole in children with rheumatoid arthritis.

C. Griscelli, A. Prieur, D. Buriot, 1978, Jornal de Pediatria.

[Chemotherapy and ovarian function. Retrospective analysis in 17 girls treated for malignant tumor or hematologic disease].

C. Griscelli, G. Schaison, R. Brauner, 1986, Archives francaises de pediatrie.

Self Education after Mismatched HLA Haploidentical Bone Marrow Transplantation

C. Griscelli, A. Fischer, J. D. Villartay, 1985 .

PROSPECTIVE STUDY OF THE OCCURRENCE OF MONOCLONAL GAMMAPATHIES FOLLOWING BONE MARROW TRANSPLANTATION IN YOUNG CHILDREN

A. Fischer, F. Deist, C. Griscelli, 1990, Transplantation.

Separation of a population of human T lymphocytes that bind prostaglandin E2 and exert a suppressor activity.

C. Griscelli, A. Durandy, F. Le Deist, 1985, Journal of immunology.

High dose immunoglobulin therapy in severe juvenile chronic arthritis: long-term follow-up in 16 patients.

C. Griscelli, A. Prieur, M. Debré, 1990, Clinical and experimental rheumatology.

[Chronic neutropenia and Crohn's disease in childhood. Report of 2 cases ].

C. Griscelli, C. Ricour, J. Vannier, 1982, Archives francaises de pediatrie.

Immediate postnatal decontamination as a means of obtaining axenic animals and human infants.

C. Griscelli, P. Raibaud, R. Ducluzeau, 1976, Canadian journal of microbiology.

Immunodeficiency associated with defective expression of the T-cell receptor-CD3 complex.

C. Griscelli, F. Le Deist, A. Fischer, 1990, The New England journal of medicine.

Country profile. France.

B. Guiraud-Chaumeil, C. Griscelli, Y. Matillon, 1997, Lancet.

[Nosologic aspects of systemic forms of very-early-onset juvenile arthritis. Apropos of 17 cases].

C. Griscelli, A. Prieur, 1983, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris.

[Nosologic aspects of systemic forms of very early onset juvenile arthritis. Apropos of 17 cases].

C. Griscelli, A. Prieur, 1983, Annales de pediatrie.

Anti‐IgA Antibodies in Childhood

C. Griscelli, B. Geny, D. Frommel, 1974, Vox sanguinis.

[Activation by injectable gamma globulins of the suppressive functions of the humoral response tested in vitro].

C. Griscelli, A. Durandy, 1983, Presse medicale.

Active suppression of B lymphocyte maturation by two different newborn T lymphocyte subsets.

C. Griscelli, A. Durandy, A. Fischer, 1979, Journal of immunology.

SMOULDERING T LYMPHOMA RELATED TO HTLV-I IN A SICILIAN CHILD

A. Fischer, F. Deist, C. Griscelli, 1985, The Lancet.

Still's disease and haemophagocytic syndrome.

C. Griscelli, A. Prieur, A. Fischer, 1985, Annals of the rheumatic diseases.

[Painful disseminated fibromatosis (systemic hyalinosis): a new hereditary collagen dysplasia].

C. Griscelli, J. Saudubray, R. Girot, 1978, Archives francaises de pediatrie.

A retrospective single-center study of clinical presentation and outcome in 117 patients with severe combined immunodeficiency.

A. Fischer, C. Griscelli, A. Durandy, 1993, Immunodeficiency.

Blood histamine levels in HIV-1-infected infants and children.

C. Griscelli, S. Blanche, C. Burtin, 1990, International archives of allergy and applied immunology.

A monoclonal antibody specific for rat intestinal lymphocytes.

C. Griscelli, N. Cerf-Bensussan, A. Bhan, 1986, Journal of immunology.

Circulating antigens in immune complexes containing late-onset rubella syndrome rubella

C. Griscelli, A. Durandy, M. Tardieu, 1980 .

Intermediate-risk childhood acute lymphoblastic leukemias: amsacrine + cytosine arabinoside versus intermediate-dose methotrexate for consolidation, and 6-mercaptopurine + methotrexate + vincristine versus monthly pulses for maintenance.

G. Leverger, C. Griscelli, S. Lemerle, 1987, Haematology and blood transfusion.

Application of the study of prognostic factors to the treatment of childhood (less than 20 years old) acute lymphoblastic leukemia.

C. Griscelli, M. Weil, F. Bauters, 1980, Bulletin du cancer.

A variant of severe combined immunodeficiency with normal in vitro response to allogeneic cells and an increase in circulating B lymphocytes persisting several months after successful bone marrow graft.

C. Griscelli, J. Brouet, J. Preud’homme, 1974, Clinical and experimental immunology.

About this journal.

C. Griscelli, L. Herzenberg, D. Teller, 2012, Archives of dermatology.

DEFECTS OF IMMUNE INTERFERON SECRETION AND NATURAL KILLER ACTIVITY IN PATIENTS WITH IMMUNOLOGICAL DISORDERS

M. Lipinski, C. Griscelli, T. Tursz, 1979, The Lancet.

[Severe combined immune deficiency with hypereosinophilia. Immunologic study of 5 cases].

C. Griscelli, A. Durandy, F. Le Deist, 1985, Archives francaises de pediatrie.

Polymerase Chain Reaction for Studies of Mother to Child Transmission of HIVI in Africa

C. Griscelli, C. Bréchot, P. Paterlini, 2001 .

Chronic progressive encephalitis in children with x-linked hypogammaglobulinemia.

C. Griscelli, P. Lebon, J. Prats-Viñas, 1980, Neuropadiatrie.

Lack of prostaglandin E2-mediated monocyte suppressive activity in newborn and mothers.

C. Griscelli, A. Durandy, S. Mamas, 1982, Clinical and experimental immunology.

[Chédiak-Higashi disease (report on a new case) (author's transl)].

P. Agache, C. Griscelli, P. Deprez, 1978, Annales de dermatologie et de venereologie.

Regulation of prostaglandin E2 and plasminogen activator by various immunomodulators in human monocytes.

C. Griscelli, P. Smets, F. Homo-Delarche, 1986, Prostaglandins, leukotrienes, and medicine.

Cytokine-mediated bone resorption in patients with the hyperimmunoglobulin E syndrome.

C. Griscelli, A. Prieur, J. Launay, 1995, Clinical immunology and immunopathology.

Monoclonal antibodies specific for human and rat intestinal lymphocytes.

C. Griscelli, N. Brousse, A. Jarry, 1987, Advances in Experimental Medicine and Biology.

Combined immunodeficiency with defective expression of HLA: modulation of an abnormal HLA synthesis and functional studies.

C. Griscelli, A. Durandy, J. Virelizier, 1983, Birth defects original article series.

Metabolic abnormalities associated with congenital immune deficiencies

C. Griscelli, 1983 .

Complete adenosine deaminase (ADA) deficiency without immunodeficiency, and primary hyperoxaluria, in a 12-year-old boy.

C. Griscelli, J. Pérignon, M. Hamet, 1980, Advances in experimental medicine and biology.

A familial T-cell lymphoma with gamma delta phenotype and an original location. Possible role of chronic Epstein-Barr virus infection.

S. Schraub, C. Bodemer, F. Sigaux, 1996, Cancer.

Absence of learning difficulties in a hyperactive boy with a terminal Xp deletion encompassing the MRX49locus

R. Chadwick, A. de la Chapelle, R. Pyatt, 2001, Journal of medical genetics.

A prospective study of infants born to women seropositive for human immunodeficiency virus type 1.

C. Griscelli, C. Rouzioux, S. Blanche, 1989 .

B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?

A. Fischer, A. Munnich, C. Griscelli, 2001, Journal of medical genetics.

Molecular characterization of ataxia telangiectasia T cell clones

G. Thomas, A. Aurias, M. Stern, 1988, Human Genetics.

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

A. Fischer, L. Notarangelo, C. Griscelli, 1992, Human genetics.

Serum IgG subclass levels in primary and acquired immunodeficiency.

C. Griscelli, J. Clauvel, P. Aucouturier, 1986, Monographs in allergy.

Immunotherapy of inflammatory diseases, 2005

C. Griscelli, J. Sibilia, 2005, Expert opinion on biological therapy.

Prostaglandin E2 and plasminogen activators in human milk and their secretion by milk macrophages.

F. Deist, C. Griscelli, G. Saint-Basile, 1986, American journal of reproductive immunology and microbiology : AJRIM.

THE DISAPPEARANCE OF GERMINAL CENTERS SYNDROME IN CHILDHOOD: Report of Three Cases IN CHRONIC LYMPHADENO-HEPATO-SPLENOMEGALY

C. Griscelli, C. Nezelof, C. Maupas, 1989 .

[Post-splenectomy infections and Pneumococcus vaccination in paediatric surgery (author's transl)].

C. Griscelli, R. Roos, B. Belohradsky, 1982, Zeitschrift fur Kinderchirurgie : organ der Deutschen, der Schweizerischen und der Osterreichischen Gesellschaft fur Kinderchirurgie = Surgery in infancy and childhood.

Fine mapping of the human SCIDX1 locus at Xq12-13.1.

A. Monaco, M. Graeber, C. Griscelli, 1993, Human molecular genetics.