Ogier H - Search Results

1

Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplex.

Garel C, Baumann C, Besnard M, Ogier H, Jaeken J, Hassan M. Garel C, et al. Among authors: ogier h. Skeletal Radiol. 1998 Jan;27(1):43-5. doi: 10.1007/s002560050335. Skeletal Radiol. 1998. PMID: 9507611

2

[Failure to thrive and intestinal diseases in congenital disorders of glycosylation].

Zentilin Boyer M, de Lonlay P, Seta N, Besnard M, Pélatan C, Ogier H, Hugot JP, Faure C, Saudubray JM, Navarro J, Cézard JP. Zentilin Boyer M, et al. Among authors: ogier h. Arch Pediatr. 2003 Jul;10(7):590-5. doi: 10.1016/s0929-693x(03)00278-1. Arch Pediatr. 2003. PMID: 12907065 French.

3

Pre- and postnatal diagnosis of succinic semialdehyde dehydrogenase deficiency using enzyme and metabolite assays.

Gibson KM, Baumann C, Ogier H, Rossier E, Vollmer B, Jakobs C. Gibson KM, et al. Among authors: ogier h. J Inherit Metab Dis. 1994;17(6):732-7. doi: 10.1007/BF00712016. J Inherit Metab Dis. 1994. PMID: 7707697

4

29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype.

Monin ML, Mignot C, De Lonlay P, Héron B, Masurel A, Mathieu-Dramard M, Lenaerts C, Thauvin C, Gérard M, Roze E, Jacquette A, Charles P, de Baracé C, Drouin-Garraud V, Khau Van Kien P, Cormier-Daire V, Mayer M, Ogier H, Brice A, Seta N, Héron D. Monin ML, et al. Among authors: ogier h. Orphanet J Rare Dis. 2014 Dec 11;9:207. doi: 10.1186/s13023-014-0207-4. Orphanet J Rare Dis. 2014. PMID: 25497157 Free PMC article.

5

Adult-onset eculizumab-resistant hemolytic uremic syndrome associated with cobalamin C deficiency.

Cornec-Le Gall E, Delmas Y, De Parscau L, Doucet L, Ogier H, Benoist JF, Fremeaux-Bacchi V, Le Meur Y. Cornec-Le Gall E, et al. Among authors: ogier h. Am J Kidney Dis. 2014 Jan;63(1):119-23. doi: 10.1053/j.ajkd.2013.08.031. Epub 2013 Nov 6. Am J Kidney Dis. 2014. PMID: 24210589

6

Infantile spasms and Menkes disease.

Sfaello I, Castelnau P, Blanc N, Ogier H, Evrard P, Arzimanoglou A. Sfaello I, et al. Among authors: ogier h. Epileptic Disord. 2000 Dec;2(4):227-30. Epileptic Disord. 2000. PMID: 11174154 Free article.

7

Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndrome.

Castelnau P, Zilbovicius M, Ribeiro MJ, Hertz-Pannier L, Ogier H, Evrard P. Castelnau P, et al. Among authors: ogier h. Pediatr Neurol. 2001 Aug;25(2):170-4. doi: 10.1016/s0887-8994(01)00295-8. Pediatr Neurol. 2001. PMID: 11551749

8

[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment].

Netter JC, Cossarizza G, Narcy C, Hubert P, Ogier H, Revillon Y, Rabier D, Saudubray JM. Netter JC, et al. Among authors: ogier h. Arch Pediatr. 1994 Aug;1(8):730-4. Arch Pediatr. 1994. PMID: 7842107 French.

9

[Clinical approach to hereditary metabolic disorders in neonates. Review of 20 years' experience].

Saudubray JM, Ogier H, Bonnefont JP, Munich A, Lombes A, Hervé F, Mitchel G, Poll The B, Specola N, Parvy B, et al. Saudubray JM, et al. Among authors: ogier h. Cesk Pediatr. 1990 Jan;45(1):1-6. Cesk Pediatr. 1990. PMID: 2393916 Czech.

10

[Research methods in metabolic myopathies in children].

Lombes A, Ogier H, Bonnefont JP, Munnich A, Saudubray JM. Lombes A, et al. Among authors: ogier h. Ann Med Interne (Paris). 1987;138(6):441-3. Ann Med Interne (Paris). 1987. PMID: 3324848 Review. French. No abstract available.

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

100 results

Search Page

Filters