Heimann G - Search Results

1

A biotinidase Km variant causing late onset bilateral optic neuropathy.

Ramaekers VT, Suormala TM, Brab M, Duran R, Heimann G, Baumgartner ER. Ramaekers VT, et al. Among authors: heimann g. Arch Dis Child. 1992 Jan;67(1):115-9. doi: 10.1136/adc.67.1.115. Arch Dis Child. 1992. PMID: 1739323 Free PMC article.

2

[Juvenile optic neuropathy caused by Km variants of biotinidase].

Brab M, Ramaekers VT, Baumgartner ER, Heimann G, Reim M. Brab M, et al. Among authors: heimann g. Klin Monbl Augenheilkd. 1992 Mar;200(3):204-9. doi: 10.1055/s-2008-1045738. Klin Monbl Augenheilkd. 1992. PMID: 1315891 German.

3

Recovery from neurological deficits following biotin treatment in a biotinidase Km variant.

Ramaekers VT, Brab M, Rau G, Heimann G. Ramaekers VT, et al. Among authors: heimann g. Neuropediatrics. 1993 Apr;24(2):98-102. doi: 10.1055/s-2008-1071522. Neuropediatrics. 1993. PMID: 8352834

4

Early and late onset manifestations of cerebral vasculitis related to varicella zoster.

Häusler MG, Ramaekers VT, Reul J, Meilicke R, Heimann G. Häusler MG, et al. Among authors: heimann g. Neuropediatrics. 1998 Aug;29(4):202-7. doi: 10.1055/s-2007-973561. Neuropediatrics. 1998. PMID: 9762696

5

Central pontine myelinolysis associated with acquired folate depletion.

Ramaekers VT, Reul J, Kusenbach G, Thron A, Heimann G. Ramaekers VT, et al. Among authors: heimann g. Neuropediatrics. 1997 Apr;28(2):126-30. doi: 10.1055/s-2007-973686. Neuropediatrics. 1997. PMID: 9208415

6

Genetic disorders and cerebellar structural abnormalities in childhood.

Ramaekers VT, Heimann G, Reul J, Thron A, Jaeken J. Ramaekers VT, et al. Among authors: heimann g. Brain. 1997 Oct;120 ( Pt 10):1739-51. doi: 10.1093/brain/120.10.1739. Brain. 1997. PMID: 9365367 Review.

7

Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: a novel neurometabolic condition responding to folinic acid substitution.

Ramaekers VT, Häusler M, Opladen T, Heimann G, Blau N. Ramaekers VT, et al. Among authors: heimann g. Neuropediatrics. 2002 Dec;33(6):301-8. doi: 10.1055/s-2002-37082. Neuropediatrics. 2002. PMID: 12571785 Free article.

8

A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopa.

Ramaekers VT, Senderek J, Häusler M, Häring M, Abeling N, Zerres K, Bergmann C, Heimann G, Blau N. Ramaekers VT, et al. Among authors: heimann g. Mol Genet Metab. 2001 Jun;73(2):179-87. doi: 10.1006/mgme.2001.3187. Mol Genet Metab. 2001. PMID: 11386854 Clinical Trial.

9

Inflammatory pseudotumors of the central nervous system: report of 3 cases and a literature review.

Häusler M, Schaade L, Ramaekers VT, Doenges M, Heimann G, Sellhaus B. Häusler M, et al. Among authors: heimann g. Hum Pathol. 2003 Mar;34(3):253-62. doi: 10.1053/hupa.2003.35. Hum Pathol. 2003. PMID: 12673560 Review.

10

Reduced folate transport to the CNS in female Rett patients.

Ramaekers VT, Hansen SI, Holm J, Opladen T, Senderek J, Häusler M, Heimann G, Fowler B, Maiwald R, Blau N. Ramaekers VT, et al. Among authors: heimann g. Neurology. 2003 Aug 26;61(4):506-15. doi: 10.1212/01.wnl.0000078939.64774.1b. Neurology. 2003. PMID: 12939425

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