Elmer C - Search Results

1

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.

2

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

3

Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable types.

Verloes A, Journel H, Elmer C, Misson JP, Le Merrer M, Kaplan J, Van Maldergem L, Deconinck H, Meire F. Verloes A, et al. Among authors: elmer c. Am J Med Genet. 1993 Apr 15;46(2):132-7. doi: 10.1002/ajmg.1320460206. Am J Med Genet. 1993. PMID: 8484397 Review.

4

[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.

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

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.

7

[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.

8

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.

9

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.

10

[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.

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