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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 1
1980 2
1981 9
1982 8
1983 9
1984 3
1985 7
1986 8
1987 6
1988 4
1989 2
1990 5
1992 3
1993 6
1994 4
1995 1
1996 1
1998 1
1999 1
2000 1
2001 2
2003 1
2004 2
2008 1
2010 2
2011 1
2012 3
2013 1
2014 3
2015 2
2016 2
2017 1
2023 0

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Search Results

100 results

Results by year

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Page 1
Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.
Morris AA, Kožich V, Santra S, Andria G, Ben-Omran TI, Chakrapani AB, Crushell E, Henderson MJ, Hochuli M, Huemer M, Janssen MC, Maillot F, Mayne PD, McNulty J, Morrison TM, Ogier H, O'Sullivan S, Pavlíková M, de Almeida IT, Terry A, Yap S, Blom HJ, Chapman KA. Morris AA, et al. Among authors: ogier h. J Inherit Metab Dis. 2017 Jan;40(1):49-74. doi: 10.1007/s10545-016-9979-0. Epub 2016 Oct 24. J Inherit Metab Dis. 2017. PMID: 27778219 Free PMC article. Review.
[Medium-chain acyl-CoA-dehydrogenase (MCAD) deficiency: French consensus for neonatal screening, diagnosis, and management].
Feillet F, Ogier H, Cheillan D, Aquaviva C, Labarthe F, Baruteau J, Chabrol B, de Lonlay P, Valayanopoulos V, Garnotel R, Dobbelaere D, Briand G, Jeannesson E, Vassault A, Vianey-Saban C; SFEIM (Société française pour l’étude des erreurs innées du métabolisme). Feillet F, et al. Among authors: ogier h. Arch Pediatr. 2012 Feb;19(2):184-93. doi: 10.1016/j.arcped.2011.10.025. Epub 2012 Jan 12. Arch Pediatr. 2012. PMID: 22244319 French.
Maternal phenylketonuria: the French survey.
Feillet F, Abadie V, Berthelot J, Maurin N, Ogier H, Vidailhet M, Farriaux JP, de Parscau L. Feillet F, et al. Among authors: ogier h. Eur J Pediatr. 2004 Sep;163(9):540-6. doi: 10.1007/s00431-004-1482-1. Epub 2004 Jul 6. Eur J Pediatr. 2004. PMID: 15241684
Neurologic crises in hereditary tyrosinemia.
Mitchell G, Larochelle J, Lambert M, Michaud J, Grenier A, Ogier H, Gauthier M, Lacroix J, Vanasse M, Larbrisseau A, et al. Mitchell G, et al. Among authors: ogier h. N Engl J Med. 1990 Feb 15;322(7):432-7. doi: 10.1056/NEJM199002153220704. N Engl J Med. 1990. PMID: 2153931 Free article.
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.
[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.
New spastic paraplegia phenotype associated to mutation of NFU1.
Tonduti D, Dorboz I, Imbard A, Slama A, Boutron A, Pichard S, Elmaleh M, Vallée L, Benoist JF, Ogier H, Boespflug-Tanguy O. Tonduti D, et al. Among authors: ogier h. Orphanet J Rare Dis. 2015 Feb 8;10:13. doi: 10.1186/s13023-015-0237-6. Orphanet J Rare Dis. 2015. PMID: 25758857 Free PMC article.
100 results