Baumann N - Search Results

1

[Cerebral ischemic accidents and kidney failure in a young man].

Julien J, Lyon-Caen O, Baumann N, Baumelou A. Julien J, et al. Among authors: baumann n. Rev Neurol (Paris). 1989;145(11):813-8. Rev Neurol (Paris). 1989. PMID: 2512605 Review. French. No abstract available.

2

[Symptomatic heterozygotic adrenoleukodystrophy in adults. 10 cases].

Ménage P, Carreau V, Tourbah A, Fontaine B, Paturneau-Jouas M, Gout O, Lubetzki C, Baumann N, Lyon-Caen O. Ménage P, et al. Among authors: baumann n. Rev Neurol (Paris). 1993;149(8-9):445-54. Rev Neurol (Paris). 1993. PMID: 8009141 Review. French.

3

[Adult onset hereditary leukoencephalopathies].

Sedel F, Tourbah A, Baumann N, Fontaine B, Aubourg P, Lubetzki C, Lyon-Caen O. Sedel F, et al. Among authors: baumann n. Rev Neurol (Paris). 2005 Oct;161(10):916-31. doi: 10.1016/s0035-3787(05)85155-0. Rev Neurol (Paris). 2005. PMID: 16365621 Review. French.

4

Cognitive function in adult adrenoleukodystrophy: comparison with leukoaraiosis and multiple sclerosis.

Lyon-Caen O, Benoit N, Carreau V, Montreuil M, Menage P, Lubetzki C, Cabanis E, Iba-Zizen MT, Tourbah A, Baumann N. Lyon-Caen O, et al. Among authors: baumann n. Dev Neurosci. 1991;13(4-5):251-3. doi: 10.1159/000112169. Dev Neurosci. 1991. PMID: 1817029

5

Localized proton magnetic resonance spectroscopy in patients with adult adrenoleukodystrophy. Increase of choline compounds in normal appearing white matter.

Tourbah A, Stievenart JL, Iba-Zizen MT, Lubetzki C, Baumann N, Eymard B, Moser HW, Lyon-Caen O, Cabanis EA. Tourbah A, et al. Among authors: baumann n. Arch Neurol. 1997 May;54(5):586-92. doi: 10.1001/archneur.1997.00550170062015. Arch Neurol. 1997. PMID: 9152115

6

Ganglioside GD1b is the target antigen for a biclonal IgM in a case of sensory-motor axonal polyneuropathy: involvement of N-acetylneuraminic acid in the epitope.

Younes-Chennoufi AB, Léger JM, Hauw JJ, Preud'homme JL, Bouche P, Aucouturier P, Ratinahirana H, Lubetzki C, Lyon-Caen O, Baumann N. Younes-Chennoufi AB, et al. Among authors: baumann n. Ann Neurol. 1992 Jul;32(1):18-23. doi: 10.1002/ana.410320105. Ann Neurol. 1992. PMID: 1379422

7

Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adults.

Sedel F, Baumann N, Turpin JC, Lyon-Caen O, Saudubray JM, Cohen D. Sedel F, et al. Among authors: baumann n. J Inherit Metab Dis. 2007 Oct;30(5):631-41. doi: 10.1007/s10545-007-0661-4. Epub 2007 Aug 10. J Inherit Metab Dis. 2007. PMID: 17694356 Review.

8

Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.

Fontaine B, Rime CS, Hazan J, Dürr A, Stevanin G, Penet C, Reboul J, Agid Y, Lyon-Caen O, Baumann N, et al. Fontaine B, et al. Among authors: baumann n. Neuromuscul Disord. 1995 Jan;5(1):11-7. doi: 10.1016/0960-8966(94)e0024-3. Neuromuscul Disord. 1995. PMID: 7719135

9

[Treatment of immune deficient neuropathies with intravenous polyvalent immunoglobulins. An open study of 16 cases].

Hoang-Xuan K, Léger JM, Ben Younes-Chennoufi A, Saidi H, Bouche P, Baumann N, Brunet P. Hoang-Xuan K, et al. Among authors: baumann n. Rev Neurol (Paris). 1993;149(6-7):385-92. Rev Neurol (Paris). 1993. PMID: 8303157 Clinical Trial. French.

10

Leukoencephalopathies associated with inborn errors of metabolism in adults.

Sedel F, Tourbah A, Fontaine B, Lubetzki C, Baumann N, Saudubray JM, Lyon-Caen O. Sedel F, et al. Among authors: baumann n. J Inherit Metab Dis. 2008 Jun;31(3):295-307. doi: 10.1007/s10545-008-0778-0. Epub 2008 Feb 25. J Inherit Metab Dis. 2008. PMID: 18344012 Review.

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