Elmer C - Search Results

1

[The value of prenatal chromosomal diagnosis in cases of fetal abnormalities: results obtained in 468 pathological pregnancies].

Vamos E, Elmer C, Lévi S, el Khazen N, Donner C, Avni F, Rodesch F. Vamos E, et al. Among authors: elmer c. Rev Med Brux. 1990 Jun;11(6):231-5. Rev Med Brux. 1990. PMID: 2371470 French.

2

Lethal malformation syndrome in three siblings. A variable expression of the same entity?

Van Regemorter N, Pierquin G, Vamos E, Elmer C, Fryns JP. Van Regemorter N, et al. Among authors: elmer c. Genet Couns. 1992;3(2):121-5. Genet Couns. 1992. PMID: 1642811 No abstract available.

3

[Nanism with short limbs, dysmorphism, renal dysplasia, growth hormone deficiency with pituitary hypoplasia and psychomotor delay: a new syndrome?].

Elmer C, Van Vliet G, Heinrichs C, Toppet M, Christophe C, Perlmutter-Cremer N, Vamos E. Elmer C, et al. J Genet Hum. 1989 Dec;37(4-5):367-72. J Genet Hum. 1989. PMID: 2635713 French.

4

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts.

Telerman-Toppet N, Biarent D, Bouton JM, de Meirleir L, Elmer C, Noel S, Vamos E, DiMauro S. Telerman-Toppet N, et al. Among authors: elmer c. J Inherit Metab Dis. 1992;15(3):323-6. doi: 10.1007/BF02435967. J Inherit Metab Dis. 1992. PMID: 1383604 No abstract available.

5

Craniosynostosis in the Ullrich-Turner syndrome.

Heinrichs C, Elmer C, Derasse M, Perlmutter N, Vamos E. Heinrichs C, et al. Among authors: elmer c. Am J Med Genet. 1991 Aug 1;40(2):252. doi: 10.1002/ajmg.1320400227. Am J Med Genet. 1991. PMID: 1760044 No abstract available.

6

Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapy.

Steenhout P, Elmer C, Clercx A, Blum D, Gnat D, van Erum S, Vertongen F, Vamos E. Steenhout P, et al. Among authors: elmer c. J Inherit Metab Dis. 1990;13(1):69-75. doi: 10.1007/BF01799334. J Inherit Metab Dis. 1990. PMID: 2109150

7

[Association of the CHARGE syndrome and imperforation of the lacrymal ducts].

Bartik M, Cordonnier M, Elmer C, Mansbach A. Bartik M, et al. Among authors: elmer c. Bull Soc Belge Ophtalmol. 1990;239:11-7. Bull Soc Belge Ophtalmol. 1990. PMID: 2133526 French.

8

Ondine-Hirschsprung syndrome (Haddad syndrome). Further delineation in two cases and review of the literature.

Verloes A, Elmer C, Lacombe D, Heinrichs C, Rebuffat E, Demarquez JL, Moncla A, Adam E. Verloes A, et al. Among authors: elmer c. Eur J Pediatr. 1993 Jan;152(1):75-7. doi: 10.1007/BF02072522. Eur J Pediatr. 1993. PMID: 8444212 Review.

9

Schinzel-Giedion syndrome.

Verloes A, Moës D, Palumbo L, Elmer C, François A, Bricteux G. Verloes A, et al. Among authors: elmer c. Eur J Pediatr. 1993 May;152(5):421-3. doi: 10.1007/BF01955902. Eur J Pediatr. 1993. PMID: 8319710

10

Haemophilia and HIV infection in a Belgian center.

Toppet M, Ferster A, Elmer C, Jonckheer T, Levy J, Sprecher S, Fondu P. Toppet M, et al. Among authors: elmer c. Acta Clin Belg. 1987;42(5):394-5. Acta Clin Belg. 1987. PMID: 3425128 No abstract available.

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