de Visser M - Search Results

1

[DNA duplication in hereditary type Ia motor and sensory neuropathy (Charcot-Marie-Tooth disease)].

Hoogendijk JE, Baas F, de Visser M, Bolhuis PA. Hoogendijk JE, et al. Among authors: de visser m. Ned Tijdschr Geneeskd. 1991 Dec 21;135(51):2412-4. Ned Tijdschr Geneeskd. 1991. PMID: 1758499 Dutch. No abstract available.

2

The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2.

Hoogendijk JE, Hensels GW, Zorn I, Valentijn L, Janssen EA, de Visser M, Barker DF, Ongerboer de Visser BW, Baas F, Bolhuis PA. Hoogendijk JE, et al. Among authors: de visser m. Hum Genet. 1991 Dec;88(2):215-8. doi: 10.1007/BF00206075. Hum Genet. 1991. PMID: 1721895

3

Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17.

Defesche JC, Hoogendijk JE, de Visser M, de Visser O, Bolhuis PA. Defesche JC, et al. Among authors: de visser o, de visser m. Neurology. 1990 Sep;40(9):1450-3. doi: 10.1212/wnl.40.9.1450. Neurology. 1990. PMID: 2392234

4

[Diseases caused by mitochondrial DNA mutations].

Wijburg FA, van den Bogert C, de Visser M, Oostra RJ, Bakker PA, Bolhuis PA. Wijburg FA, et al. Among authors: de visser m. Ned Tijdschr Geneeskd. 1995 Jul 1;139(26):1322-6. Ned Tijdschr Geneeskd. 1995. PMID: 7617049 Review. Dutch. No abstract available.

5

Alternatively sized duplication in Charcot-Marie-Tooth disease type 1A.

Valentijn LJ, Baas F, Zorn I, Hensels GW, de Visser M, Bolhuis PA. Valentijn LJ, et al. Among authors: de visser m. Hum Mol Genet. 1993 Dec;2(12):2143-6. doi: 10.1093/hmg/2.12.2143. Hum Mol Genet. 1993. PMID: 8111385 No abstract available.

6

Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype.

Hoogendijk JE, De Visser M, Bolhuis PA, Hart AA, Ongerboer de Visser BW. Hoogendijk JE, et al. Among authors: de visser m. Muscle Nerve. 1994 Jan;17(1):85-90. doi: 10.1002/mus.880170112. Muscle Nerve. 1994. PMID: 8264707

7

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A.

Valentijn LJ, Baas F, Wolterman RA, Hoogendijk JE, van den Bosch NH, Zorn I, Gabreëls-Festen AW, de Visser M, Bolhuis PA. Valentijn LJ, et al. Among authors: de visser m. Nat Genet. 1992 Dec;2(4):288-91. doi: 10.1038/ng1292-288. Nat Genet. 1992. PMID: 1303281

8

Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease.

Meggouh F, de Visser M, Arts WF, De Coo RI, van Schaik IN, Baas F. Meggouh F, et al. Among authors: de visser m, de coo ri. Ann Neurol. 2005 Apr;57(4):589-91. doi: 10.1002/ana.20434. Ann Neurol. 2005. PMID: 15786462

9

Conduction block in hereditary motor and sensory neuropathy type I.

Hoogendijk JE, de Visser M, Bour LJ, Jennekens FG, Ongerboer BW. Hoogendijk JE, et al. Among authors: de visser m. Muscle Nerve. 1992 Apr;15(4):520-1; author reply 523. Muscle Nerve. 1992. PMID: 1565125 No abstract available.

10

Somatosensory evoked potentials, sensory nerve potentials and sensory nerve conduction in hereditary motor and sensory neuropathy type I.

Aramideh M, Hoogendijk JE, Aalfs CM, Posthumus Meyjes FE, De Visser M, Ongerboer de Visser BW. Aramideh M, et al. Among authors: de visser m. J Neurol. 1992 May;239(5):277-83. doi: 10.1007/BF00810353. J Neurol. 1992. PMID: 1607892

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