N. Mulliez

发表

Essential fatty acids interconversion in the human fetal liver.

G. Béréziat, J. Chambaz, D. Pépin, 1985, Biology of the neonate.

Coexpression in Humans by Kidney and Fetal Envelopes of a 280 kDa-coated Pit-restricted Protein Similarity with the Murine Teratogenic Antibodies Target of

P. Verroust, D. Sahali, P. Ronco, 2007 .

Fetoacinar pancreatic protein in the developing human pancreas.

M. Nap, N. Mulliez, G. Albers, 1987, Differentiation; research in biological diversity.

Role of cholesterol in embryonic development.

F. Chevy, C. Wolf, C. Wolf, 2000, The American journal of clinical nutrition.

Antibodies to the 280-kd coated pit protein, target of teratogenic antibodies, produce alterations in the traffic of internalized proteins.

P. Verroust, M. Galcerán, S. Le Panse, 1994, The American journal of pathology.

Changes in serum sterols of rats treated with 7-dehydrocholesterol-delta 7-reductase inhibitors: comparison to levels in humans with Smith-Lemli-Opitz syndrome.

F. Chevy, C. Wolf, M. Kolf‐Clauw, 1996, Journal of lipid research.

Pseudo-meconium ileus due to cytomegalovirus infection: a report of three cases.

R. Bouvier, D. Lémery, P. Dechelotte, 1992, Pediatric pathology.

Role of cholesterol in embryonic development 1 – 4

F. Chevy, C. Wolf, D. Citadelle, 2000 .

Cholesterol biosynthesis inhibited by BM15.766 induces holoprosencephaly in the rat.

F. Chevy, C. Wolf, M. Kolf‐Clauw, 1997, Teratology.

VIP and histamine H2 receptor activity in human fetal gastric glands

M. Gonzalès, C. Gespach, E. Chastre, 1986, Experientia.

Comparative immunochemistry and ontogeny of two closely related coated pit proteins. The 280-kd target of teratogenic antibodies and the 330-kd target of nephritogenic antibodies.

J. Sabourin, P. Verroust, D. Sahali, 1993, The American journal of pathology.

Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

C. Moraine, M. Merrer, C. Moraine, 1988, Journal of medical genetics.

Lethal familial fetal akinesia sequence (FAS) with distinct neuropathological pattern: type III lissencephaly syndrome.

M. Gonzalès, J. Roume, N. Mulliez, 1996, American journal of medical genetics.

Radiographic, haematological, and biochemical findings in a fetus with Caffey disease

M. Gonzalès, R. Afriat, N. Mulliez, 1992, Prenatal diagnosis.

Frequency of early in utero HIV‐1 infection: a blind DNA polymerase chain reaction study on 100 fetal thymuses

H. Agut, J. Roume, C. Bréchot, 1995, AIDS.

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

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

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

N. Philip, A. Verloes, M. Gonzalès, 1991, Journal of medical genetics.

Fetal hydrocephalus. Clinical significance of associated anomalies and genetic counseling: a pathological approach.

M. Gonzalès, J. Roume, N. Mulliez, 1990, Genetic counseling.

Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature.

L. Koulischer, A. Verloes, M. Gonzalès, 1992, American journal of medical genetics.

Dermatopathological aspects of restrictive dermopathy

A. Verloes, G. Piérard, C. Piérard‐franchimont, 1992, The Journal of pathology.

Serotonin deficiency in phenylketonuria embryopathy.

J. Launay, D. Citadelle, M. Madani, 1995, Toxicology in vitro : an international journal published in association with BIBRA.

An animal model for maternal phenylketonuria.

A. Munnich, S. Lyonnet, S. Nizard, 1991, Journal of medical genetics.

Vasoactive intestinal peptide receptor activity in human fetal enterocytes

C. Gespach, E. Chastre, S. Emami, 1985, FEBS letters.

[Toxoplasmosis and pregnancy. Evaluation of 2 years of prevention of congenital toxoplasmosis in the maternity ward of Hôpital Saint-Antoine (1973-1974)].

N. Mulliez, A. Herbillon, D. Marmor, 1976, Journal de gynecologie, obstetrique et biologie de la reproduction.

Cardiovascular abnormalities in thoracopagus twins: embryological interpretation and review.

M. Gonzalès, G. Bloch, N. Benhaiem-Sigaux, 1987, Early human development.

Characterization of a 280-kD protein restricted to the coated pits of the renal brush border and the epithelial cells of the yolk sac. Teratogenic effect of the specific monoclonal antibodies

P. Verroust, D. Sahali, P. Ronco, 1988, The Journal of experimental medicine.

Correlation between HIV infection and central nervous system (CNS) changes in fetal brain.

J. Roume, F. Encha-Razavi, R. Vazeux, 1991, Journal of Acquired Immune Deficiency Syndromes.

Congenital hypothalamic hamartoma syndrome: nosological discussion and minimum diagnostic criteria of a possibly familial form.

M. Gonzalès, J. Roume, F. Encha-Razavi, 1992, American journal of medical genetics.

Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

M. Merrer, C. Moraine, M. Imbert, 1988, Journal of medical genetics.

Coexpression in humans by kidney and fetal envelopes of a 280 kDa-coated pit-restricted protein. Similarity with the murine target of teratogenic antibodies.

P. Verroust, D. Sahali, C. Laurent‐Winter, 1992, The American journal of pathology.

Intrauterine transmission of human herpesvirus 6

H. Agut, L. Poirel, J. Roume, 1992, The Lancet.