G. Malpuech

发表

Study of final height in Turner's syndrome: ethnic and genetic influences.

C. Sultan, J. Limal, G. Simonin, 1994, Acta paediatrica.

Enteroadherent Escherichia coli and diarrhea in children: a prospective case-control study

C. Le Bouguénec, C. Forestier, B. Joly, 1996, Journal of clinical microbiology.

Isolated familial adrenocorticotropin deficiency: prenatal diagnosis by maternal plasma estriol assay.

A. Labbé, P. Dechelotte, J. M. Optiz, 1988, American journal of medical genetics.

An outbreak due to echovirus type 30 in a neonatal unit in France in 1997: usefulness of PCR diagnosis.

A. Labbé, J. Bailly, M. Chambon, 1999, The Journal of hospital infection.

Echocardiographic patterns in infants and children with chronic renal failure.

J. Cassagnes, J. Gourgand, J. Palcoux, 1982, The International journal of pediatric nephrology.

Familial Growth Retardation with Isolated Thyroid-Stimulating Hormone Deficiency

A. Labbé, C. Dubray, G. Besse, 1984, Clinical pediatrics.

Serum neuron‐specific/nonneuronal enolase ratio in the diagnosis of neuroblastomas

B. Dastugue, O. Hartmann, J. Lemerle, 1988, Cancer.

Fraser syndrome with renal agenesis in two consanguineous Turkish families.

P. Lefrançois, C. Francannet, P. Dechelotte, 1990, American journal of medical genetics.

Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.

P. Donohoue, M. Fassnacht, L. Dunkel, 2005, The Journal of clinical endocrinology and metabolism.

[Adrenal hypoplasia congenita: four new cases in children].

M. Forest, M. Nicolino, F. Prieur, 2005, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Contribution of electron microscopy of cultures of fibroblasts in the diagnosis of hereditary metabolic diseases].

A. Labbé, P. Malet, P. Rousseau, 1986, Pathologie-biologie.

[Congenital subclavian steal syndrome].

E. Raynaud, G. Malpuech, F. Petetin, 1972, Pediatrie.

[Familial cerebral gigantism. A new case with autosomal dominant transmission?].

G. Malpuech, P. Goumy, M. Gannat, 1979, Pediatrie.

[Simultaneous revelation of acute lymphoblastic leukemia and infectious mononucleosis].

D. Beytout, E. Raynaud, G. Malpuech, 1973, Pediatrie.

Congenital adrenal hypoplasia due to isolated familial ACTH deficiency.

A. Beaufrère, A. Labbé, C. Darcha, 1994, Pediatric pathology.

Evaluation of erythropoietic/hematopoietic reconstitution after BMT by highly fluorescent reticulocyte counts compares favorably with traditional peripheral blood cell counting.

J. Kanold, F. Demeocq, P. Travade, 1993, Bone marrow transplantation.

Safe and efficient peripheral blood stem cell collection in the smallest of children.

M. Berger, P. Lutz, D. Plantaz, 1998, Therapeutic apheresis : official journal of the International Society for Apheresis and the Japanese Society for Apheresis.

Pulmonary hyperplasia in Fraser syndrome

A. Labbé, D. Lémery, P. Dechelotte, 1992, Pediatric Pulmonology.

Use of G‐CSF alone to mobilize peripheral blood stem cells for collection from children

M. Berger, P. Lutz, D. Plantaz, 1994, British journal of haematology.

[Early infantile, cholestatic, rapidly-fatal form of type C sphingomyelinosis. 2 cases].

R. Rousson, M. Vanier, P. Guibaud, 1979, Pediatrie.

Kinetics of hematopoietic progenitor cell release induced by G-CSF-alone in children with solid tumors and leukemias

M. Berger, P. Lutz, D. Plantaz, 1998, Bone Marrow Transplantation.

[Meckel's syndrome: an unusual pedigree].

B. Dalens, J. Palcoux, G. Malpuech, 1979, Journal de genetique humaine.

A dynamic study in two new cases of X chromosome translocations

M. Mattei, J. Mattéi, F. Giraud, 1978, Human Genetics.

Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.

J. Drouin, C. Deal, A. Pulichino, 2003, Genes & development.

[Anhidrotic ectodermal dysplasia. Value of early diagnosis].

J. Palcoux, J. Gaulme, G. Malpuech, 1980, Pediatrie.

Plasma exchange in Rasmussen's encephalitis.

M. Tardieu, G. Sébire, Y. Loriette, 1997, Therapeutic apheresis : official journal of the International Society for Apheresis and the Japanese Society for Apheresis.

Two‐step immunoablative treatment with autologous peripheral blood CD34+ cell transplantation in an 8‐year‐old boy with autoimmune haemolytic anaemia

M. Berger, C. Paillard, K. Yakouben, 2000, British journal of haematology.

[Trisomy 8 with mosaicism].

B. Dutrillaux, Y. Fonck, J. Gaulme, 1972, Archives francaises de pediatrie.

[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12].

C. Junien, R. Tenconi, J. Lejeune, 1976, Annales de genetique.

A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.

F. Demeocq, P. Vanlieferinghen, J. Palcoux, 1983, American journal of medical genetics.

Male pseudohermaphroditism, partial androgen receptors defect, 11p13 deletion: indication of gene localization

J. Opitz, C. Sultan, C. Francannet, 1986 .

X-linked mental retardation with isolated growth hormone deficiency is mapped to Xq22-Xq27.2 in one family.

M. Raynaud, C. Francannet, N. Ronce, 1998, American journal of medical genetics.

Complete androgen insensitivity syndrome due to a new frameshift deletion in exon 4 of the androgen receptor gene: functional analysis of the mutant receptor

A. Brinkmann, S. Lumbroso, V. Georget, 1995, Molecular and Cellular Endocrinology.

Retrospective case-control study of diffusely adhering Escherichia coli and clinical features in children with diarrhea

C. Forestier, C. Jallat, C. Rich, 1995, Journal of clinical microbiology.

[Neuroblastoma in the Auvergne region from 1986 to 1991: epidemiological data].

J. Chazal, P. Chopard, P. Dechelotte, 1993, Pediatrie.

Metachromatic leukodystrophy. Ultrastructural and enzymatic study of a case of variant O form.

N. Baumann, R. Escourolle, J. Turpin, 1975, Archives of neurology.

[Trisomy of the short arm of 9 with isochromosome 9p and partial monosomy Yq].

A. Geneix, P. Malet, M. O. Roland, 1983, Annales de genetique.

NM1 keratinocytes display biochemical markers of keratinization.

J. de Grouchy, J. Thivolet, M. Faure, 1989, The Journal of investigative dermatology.

Hypomagensemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint

J. Mandel, C. Philippe, A. Hanauer, 1994, Human Genetics.

[Malassezia furfur septicemia after bone marrow graft].

F. Demeocq, H. Carla, D. Girault, 1995, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Complete deletion of the short arm of chromosome 18 and G-18 translocation with dyschromy and hypothyroidism].

J. Gaulme, E. Raynaud, G. Malpuech, 1971, Archives francaises de pediatrie.

BRCA1 and BRCA2 protein expressions in an ovotestis of a 46, XX true hermaphrodite

Y. Bignon, L. Cravello, P. Dechelotte, 2000, Breast Cancer Research.

Comparison of different treatment regimens in a case of homozygous familial hypercholesterolemia.

P. Vanlieferinghen, J. Palcoux, P. Jouanel, 2002, Therapeutic apheresis : official journal of the International Society for Apheresis and the Japanese Society for Apheresis.