Saudubray JM - Search Results

1

Quéré I, Simorre B, Ruivard M, Le Hello C, Parrot F, Mégnien JL, Touati G, Chassé JF, Saudubray JM, Zittoun J. Quéré I, et al. Among authors: saudubray jm. Rev Med Interne. 2001 Dec;22 Suppl 3:347s-355s. Rev Med Interne. 2001. PMID: 11794879 Review. French.

2

[Vascular complications of homocystinuria: a retrospective multicenter study].

Simorre B, Quéré I, Berrut G, Chassé JF, Bellet H, Kamoun P, le Hello C, Saudubray JM, Janbon C. Simorre B, et al. Among authors: saudubray jm. Rev Med Interne. 2002 Mar;23(3):267-72. doi: 10.1016/s0248-8663(01)00551-3. Rev Med Interne. 2002. PMID: 11928374 French.

3

[Hereditary metabolic causes of stroke and pseudo-stroke in adulthood].

Nassogne MC, Touati G, Beyler C, Saudubray JM. Nassogne MC, et al. Among authors: saudubray jm. Rev Med Interne. 2001 Dec;22 Suppl 3:338s-346s. Rev Med Interne. 2001. PMID: 11794878 Review. French.

4

Evidence of carotid artery wall hypertrophy in homozygous homocystinuria.

Megnien JL, Gariepy J, Saudubray JM, Nuoffer JM, Denarie N, Levenson J, Simon A. Megnien JL, et al. Among authors: saudubray jm. Circulation. 1998 Nov 24;98(21):2276-81. doi: 10.1161/01.cir.98.21.2276. Circulation. 1998. PMID: 9826314

5

Remethylation defects: guidelines for clinical diagnosis and treatment.

Ogier de Baulny H, Gérard M, Saudubray JM, Zittoun J. Ogier de Baulny H, et al. Among authors: saudubray jm. Eur J Pediatr. 1998 Apr;157 Suppl 2:S77-83. doi: 10.1007/pl00014307. Eur J Pediatr. 1998. PMID: 9587031 Review.

6

[Hereditary metabolic diseases in adults].

Saudubray JM, Nuoffer JM, de Lonlay P, Castelnau P, Touati G. Saudubray JM, et al. Rev Med Interne. 1998;19 Suppl 3:366S-375S. Rev Med Interne. 1998. PMID: 9885858 Review. French. No abstract available.

7

Relations between molecular and biological abnormalities in 11 families from siblings affected with methylenetetrahydrofolate reductase deficiency.

Tonetti C, Saudubray JM, Echenne B, Landrieu P, Giraudier S, Zittoun J. Tonetti C, et al. Among authors: saudubray jm. Eur J Pediatr. 2003 Jul;162(7-8):466-475. doi: 10.1007/s00431-003-1196-9. Epub 2003 May 6. Eur J Pediatr. 2003. PMID: 12733064

8

Clinical approach to inherited metabolic disorders in neonates: an overview.

Saudubray JM, Nassogne MC, de Lonlay P, Touati G. Saudubray JM, et al. Semin Neonatol. 2002 Feb;7(1):3-15. doi: 10.1053/siny.2001.0083. Semin Neonatol. 2002. PMID: 12069534 Review.

9

Severe hypoglycaemia in isolated 3-methylcrotonyl-CoA carboxylase deficiency; a rare, severe clinical presentation.

Oude Luttikhuis HG, Touati G, Rabier D, Williams M, Jakobs C, Saudubray JM. Oude Luttikhuis HG, et al. Among authors: saudubray jm. J Inherit Metab Dis. 2005;28(6):1136-8. doi: 10.1007/s10545-005-4545-1. J Inherit Metab Dis. 2005. PMID: 16435207

10

Persistent hyperinsulinaemic hypoglycaemia.

de Lonlay P, Touati G, Robert JJ, Saudubray JM. de Lonlay P, et al. Among authors: saudubray jm. Semin Neonatol. 2002 Feb;7(1):95-100. doi: 10.1053/siny.2001.0090. Semin Neonatol. 2002. PMID: 12069542 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

434 results

Search Page

Filters