Metz C - Search Results

1

[Prevalence of vitamin D deficiency in children aged 5-10 years in western Brittany].

Beuzit C, L'Hour MC, Roudaut S, Gouillou M, Metz C, Moineau MP, Kerspern H, de Parscau L, Teissier R. Beuzit C, et al. Among authors: metz c. Arch Pediatr. 2015 Nov;22(11):1112-8. doi: 10.1016/j.arcped.2015.08.013. Epub 2015 Oct 9. Arch Pediatr. 2015. PMID: 26482185 French.

2

[Neonatal detection of central hypothyroidism].

Giroux B, Metz C, Giroux JD, de Parscau L. Giroux B, et al. Among authors: metz c. Arch Pediatr. 1997 Jun;4(6):542-6. doi: 10.1016/s0929-693x(97)87576-8. Arch Pediatr. 1997. PMID: 9239270 French.

3

[Transitory hyperinsulinism with hypoglycemia in asphyxia neonatorum].

Giroux JD, Vernotte E, Gagneur A, Metz C, Collet M, de Parscau L. Giroux JD, et al. Among authors: metz c. Arch Pediatr. 1997 Dec;4(12):1213-6. doi: 10.1016/s0929-693x(97)82612-7. Arch Pediatr. 1997. PMID: 9538426 French.

4

[Hypophyseal central hypothyroidism due to isolated TSH deficiency. Apropos of a familial neonatal case].

Giroux B, Metz C, Giroux JD, de Parscau L. Giroux B, et al. Among authors: metz c. Arch Pediatr. 1997 Nov;4(11):1146-8. doi: 10.1016/s0929-693x(97)88990-7. Arch Pediatr. 1997. PMID: 9488755 French. No abstract available.

5

[Neonatal diabetes mellitus associated with an autoimmune disease].

Finel E, Giroux JD, Metz C, Robert JJ, Robert O, Sadoun E, Alix D, de Parscau L. Finel E, et al. Among authors: metz c. Arch Pediatr. 1996 Aug;3(8):782-4. doi: 10.1016/0929-693x(96)82160-9. Arch Pediatr. 1996. PMID: 8998531 French.

6

Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1.

Hubert EL, Teissier R, Fernandes-Rosa FL, Fay M, Rafestin-Oblin ME, Jeunemaitre X, Metz C, Escoubet B, Zennaro MC. Hubert EL, et al. Among authors: metz c. J Am Soc Nephrol. 2011 Nov;22(11):1997-2003. doi: 10.1681/ASN.2011030245. Epub 2011 Sep 8. J Am Soc Nephrol. 2011. PMID: 21903996 Free PMC article.

7

[Intraventricular hemorrhage in utero].

Gautier A, Metz C, Chabaud JJ, Le Guern H, Alix D, Boog G, Lyon G. Gautier A, et al. Among authors: metz c. Arch Fr Pediatr. 1990 Jun-Jul;47(6):429-31. Arch Fr Pediatr. 1990. PMID: 2206105 Review. French.

8

The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.

Marcos S, Sarfati J, Leroy C, Fouveaut C, Parent P, Metz C, Wolczynski S, Gérard M, Bieth E, Kurtz F, Verier-Mine O, Perrin L, Archambeaud F, Cabrol S, Rodien P, Hove H, Prescott T, Lacombe D, Christin-Maitre S, Touraine P, Hieronimus S, Dewailly D, Young J, Pugeat M, Hardelin JP, Dodé C. Marcos S, et al. Among authors: metz c. J Clin Endocrinol Metab. 2014 Oct;99(10):E2138-43. doi: 10.1210/jc.2014-2110. Epub 2014 Jul 31. J Clin Endocrinol Metab. 2014. PMID: 25077900

9

[Transient hypothyroidism after iodine opacification of epicutaneo-caval catheters in neonatal intensive care].

Giroux JD, Sizun J, Rubio S, Metz C, Montaud N, Guillois B, Alix D. Giroux JD, et al. Among authors: metz c. Arch Fr Pediatr. 1993 Mar;50(3):273. Arch Fr Pediatr. 1993. PMID: 8338426 French. No abstract available.

10

Detection of an unexpected subtelomeric 15q26.2 --> qter deletion in a little girl: clinical and cytogenetic studies.

Pinson L, Perrin A, Plouzennec C, Parent P, Metz C, Collet M, Le Bris MJ, Douet-Guilbert N, Morel F, De Braekeleer M. Pinson L, et al. Among authors: metz c. Am J Med Genet A. 2005 Oct 1;138A(2):160-5. doi: 10.1002/ajmg.a.30939. Am J Med Genet A. 2005. PMID: 16114049 Review.

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