Mulliez N - Search Results

1

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

Encha-Razavi F, Larroche JC, Roume J, Migne G, Delezoide AL, Gonzales M, Mulliez N. Encha-Razavi F, et al. Among authors: mulliez n. Am J Med Genet. 1992 Jan 1;42(1):44-50. doi: 10.1002/ajmg.1320420111. Am J Med Genet. 1992. PMID: 1308364

2

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

Encha Razavi F, Larroche JC, Roume J, Gonzales M, Kondo HC, Mulliez N. Encha Razavi F, et al. Among authors: mulliez n. Am J Med Genet. 1996 Mar 1;62(1):16-22. doi: 10.1002/(SICI)1096-8628(19960301)62:1<16::AID-AJMG4>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8779318

3

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

Verloes A, Mulliez N, Gonzales M, Laloux F, Hermanns-Lê T, Piérard GE, Koulischer L. Verloes A, et al. Among authors: mulliez n. Am J Med Genet. 1992 Jun 1;43(3):539-47. doi: 10.1002/ajmg.1320430308. Am J Med Genet. 1992. PMID: 1605246 Review.

4

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

Verloes A, Aymé S, Gambarelli D, Gonzales M, Le Merrer M, Mulliez N, Philip N, Roume J. Verloes A, et al. Among authors: mulliez n. J Med Genet. 1991 May;28(5):297-303. doi: 10.1136/jmg.28.5.297. J Med Genet. 1991. PMID: 1865466 Free PMC article. Review.

5

[Neuropathological study of 134 fetuses in HIV infected mother].

Encha-Razavi F, Larroche JC, Roume J, Mulliez N, Lescs MC. Encha-Razavi F, et al. Among authors: mulliez n. Arch Anat Cytol Pathol. 1997;45(2-3):118-20. Arch Anat Cytol Pathol. 1997. PMID: 9382602 French.

6

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

Encha-Razavi F, Larroche JC, Vazeux R, Roume J, Mulliez N. Encha-Razavi F, et al. Among authors: mulliez n. J Acquir Immune Defic Syndr (1988). 1991;4(5):540. J Acquir Immune Defic Syndr (1988). 1991. PMID: 2016691 No abstract available.

7

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

Roume J, Larroche JC, Razavi-Encha F, Gonzales M, Migne G, Mulliez N. Roume J, et al. Among authors: mulliez n. Genet Couns. 1990;1(3-4):185-96. Genet Couns. 1990. PMID: 2098043

8

[Role of the pathologist in prenatal diagnosis and genetic counselling].

Roume J, Gonzales M, Mulliez N. Roume J, et al. Among authors: mulliez n. Ann Pathol. 1997 Sep;17(4):236-9. Ann Pathol. 1997. PMID: 9409882 Review. French. No abstract available.

9

[The incidence of congenital malformations. A five-year study carried out in a Paris maternity unit (author's transl)].

Roux C, Migne G, Mulliez N, Youssef S. Roux C, et al. Among authors: mulliez n. J Gynecol Obstet Biol Reprod (Paris). 1982;11(2):215-26. J Gynecol Obstet Biol Reprod (Paris). 1982. PMID: 7108154 French.

10

Copper in human fetal tissues.

Kamoun P, Gonzales M, Mulliez N. Kamoun P, et al. Among authors: mulliez n. Eur J Pediatr. 1989 Apr;148(6):581. doi: 10.1007/BF00441568. Eur J Pediatr. 1989. PMID: 2744026 No abstract available.

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