Ogier HA - Search Results

1

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

Poll-The BT, Saudubray JM, Ogier HA, Odièvre M, Scotto JM, Monnens L, Govaerts LC, Roels F, Cornelis A, Schutgens RB, et al. Poll-The BT, et al. Among authors: ogier ha. Eur J Pediatr. 1987 Sep;146(5):477-83. doi: 10.1007/BF00441598. Eur J Pediatr. 1987. PMID: 2445576

2

Impaired plasmalogen metabolism in infantile Refsum's disease.

Poll-Thé BT, Ogier H, Saudubray JM, Schutgens RB, Wanders RJ, van den Bosch H, Schrakamp G. Poll-Thé BT, et al. Eur J Pediatr. 1986 Feb;144(5):513-4. doi: 10.1007/BF00441753. Eur J Pediatr. 1986. PMID: 2420599 No abstract available.

3

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).

Poll-The BT, Roels F, Ogier H, Scotto J, Vamecq J, Schutgens RB, Wanders RJ, van Roermund CW, van Wijland MJ, Schram AW, et al. Poll-The BT, et al. Am J Hum Genet. 1988 Mar;42(3):422-34. Am J Hum Genet. 1988. PMID: 2894756 Free PMC article.

4

Antenatal diagnosis of infantile Refsum's disease.

Poll-The BT, Poulos A, Sharp P, Boue J, Ogier H, Odièvre M, Saudubray JM. Poll-The BT, et al. Clin Genet. 1985 May;27(5):524-6. doi: 10.1111/j.1399-0004.1985.tb00246.x. Clin Genet. 1985. PMID: 2408795 No abstract available.

5

Absence of hepatic peroxisomes in a case of infantile Refsum's disease.

Ogier H, Roels F, Cornelis A, Poll The BT, Scotto JM, Odievre M, Sandubray JM. Ogier H, et al. Scand J Clin Lab Invest. 1985 Dec;45(8):767-8. doi: 10.3109/00365518509155292. Scand J Clin Lab Invest. 1985. PMID: 2417305 No abstract available.

6

Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction.

Poll-The BT, Saudubray JM, Ogier H, Schutgens RB, Wanders RJ, Schrakamp G, van den Bosch H, Trijbels JM, Poulos A, Moser HW, et al. Poll-The BT, et al. J Inherit Metab Dis. 1986;9(2):169-74. doi: 10.1007/BF01799455. J Inherit Metab Dis. 1986. PMID: 2427795

7

Hepatic peroxisomes are deficient in infantile refsum disease: a cytochemical study of 4 cases.

Roels F, Cornelis A, Poll-The BT, Aubourg P, Ogier H, Scotto J, Saudubray JM. Roels F, et al. Am J Med Genet. 1986 Oct;25(2):257-71. doi: 10.1002/ajmg.1320250210. Am J Med Genet. 1986. PMID: 2430454

8

de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency.

Ogier H, Lombes A, Scholte HR, Poll-The BT, Fardeau M, Alcardi J, Vignes B, Niaudet P, Saudubray JM. Ogier H, et al. J Pediatr. 1988 May;112(5):734-9. doi: 10.1016/s0022-3476(88)80690-5. J Pediatr. 1988. PMID: 2834526

9

Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: cytochemical and morphometric data.

Roels F, Pauwels M, Poll-Thé BT, Scotto J, Ogier H, Aubourg P, Saudubray JM. Roels F, et al. Virchows Arch A Pathol Anat Histopathol. 1988;413(4):275-85. doi: 10.1007/BF00783019. Virchows Arch A Pathol Anat Histopathol. 1988. PMID: 3140473

10

[Research methods in metabolic myopathies in children].

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

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