Steiner I - Search Results

1

Family with inflammatory demyelinating polyneuropathy and the HNPP 17p12 deletion.

Korn-Lubetzki I, Argov Z, Raas-Rothschild A, Wirguin I, Steiner I. Korn-Lubetzki I, et al. Among authors: steiner i. Am J Med Genet. 2002 Dec 1;113(3):275-8. doi: 10.1002/ajmg.10725. Am J Med Genet. 2002. PMID: 12439896

2

Chronic inflammatory demyelinating polyneuropathy presenting with features of GBS.

Korn-Lubetzki I, Steiner I. Korn-Lubetzki I, et al. Among authors: steiner i. Neurology. 2002 Dec 10;59(11):1823-4; author reply 1824. doi: 10.1212/wnl.59.11.1823-a. Neurology. 2002. PMID: 12473792 No abstract available.

3

[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy].

Korn-Lubetzki I, Steiner I. Korn-Lubetzki I, et al. Among authors: steiner i. Rev Neurol (Paris). 2005 Sep;161(8-9):848; author reply 848-9. doi: 10.1016/s0035-3787(05)85147-1. Rev Neurol (Paris). 2005. PMID: 16244570 French. No abstract available.

4

Recurrence of Sydenham chorea: implications for pathogenesis.

Korn-Lubetzki I, Brand A, Steiner I. Korn-Lubetzki I, et al. Among authors: steiner i. Arch Neurol. 2004 Aug;61(8):1261-4. doi: 10.1001/archneur.61.8.1261. Arch Neurol. 2004. PMID: 15313844

5

The occurrence of Guillain-Barré syndrome within families.

Korn-Lubetzki I, Steiner I. Korn-Lubetzki I, et al. Among authors: steiner i. Neurology. 2005 May 10;64(9):1665-6; author reply 1665-6. doi: 10.1212/wnl.64.9.1665. Neurology. 2005. PMID: 15883350 No abstract available.

6

Progressive dystonia with optic atrophy in a Jewish-Iraqi family.

Korn-Lubetzki I, Blumenfeld A, Gomori JM, Soffer D, Steiner I. Korn-Lubetzki I, et al. Among authors: steiner i. J Neurol Sci. 1997 Oct 3;151(1):57-63. doi: 10.1016/s0022-510x(97)00106-8. J Neurol Sci. 1997. PMID: 9335011

7

Multiple sclerosis--in need of a critical reappraisal.

Steiner I, Wirguin I. Steiner I, et al. Med Hypotheses. 2000 Jan;54(1):99-106. doi: 10.1054/mehy.1998.0835. Med Hypotheses. 2000. PMID: 10790735

8

Increased severity over generations of Charcot-Marie-Tooth disease type 1A.

Steiner I, Gotkine M, Steiner-Birmanns B, Biran I, Silverstein S, Abeliovich D, Argov Z, Wirguin I. Steiner I, et al. Among authors: steiner birmanns b. J Neurol. 2008 Jun;255(6):813-9. doi: 10.1007/s00415-008-0693-1. Epub 2008 Apr 30. J Neurol. 2008. PMID: 18438698

9

Sensory peripheral neuropathy of vitamin B12 deficiency: a primary demyelinating disease?

Steiner I, Kidron D, Soffer D, Wirguin I, Abramsky O. Steiner I, et al. J Neurol. 1988 Jan;235(3):163-4. doi: 10.1007/BF00314308. J Neurol. 1988. PMID: 2835439

10

Mutation in the methylenetetrahydrofolate reductase gene might be a risk factor for cerebrovascular disease in peripartum and under oral contraceptive use.

Korn-Lubetzki I, Gillis S, Steiner I. Korn-Lubetzki I, et al. Among authors: steiner i. Eur Neurol. 2001;45(3):171-3. doi: 10.1159/000052117. Eur Neurol. 2001. PMID: 11306861

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