Hoogendijk JE - Search Results

1

Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutation.

Bienfait HM, Faber CG, Baas F, Gabreëls-Festen AA, Koelman JH, Hoogendijk JE, Verschuuren JJ, Wokke JH, de Visser M. Bienfait HM, et al. Among authors: hoogendijk je. J Neurol Neurosurg Psychiatry. 2006 Apr;77(4):534-7. doi: 10.1136/jnnp.2005.073437. J Neurol Neurosurg Psychiatry. 2006. PMID: 16543539 Free PMC article.

2

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A.

Valentijn LJ, Bolhuis PA, Zorn I, Hoogendijk JE, van den Bosch N, Hensels GW, Stanton VP Jr, Housman DE, Fischbeck KH, Ross DA, et al. Valentijn LJ, et al. Among authors: hoogendijk je. Nat Genet. 1992 Jun;1(3):166-70. doi: 10.1038/ng0692-166. Nat Genet. 1992. PMID: 1303229

3

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: hoogendijk je. Nat Genet. 1992 Dec;2(4):288-91. doi: 10.1038/ng1292-288. Nat Genet. 1992. PMID: 1303281

4

De-novo mutation in hereditary motor and sensory neuropathy type I.

Hoogendijk JE, Hensels GW, Gabreëls-Festen AA, Gabreëls FJ, Janssen EA, de Jonghe P, Martin JJ, van Broeckhoven C, Valentijn LJ, Baas F, et al. Hoogendijk JE, et al. Lancet. 1992 May 2;339(8801):1081-2. doi: 10.1016/0140-6736(92)90668-s. Lancet. 1992. PMID: 1349106

5

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. Muscle Nerve. 1992 Apr;15(4):520-1; author reply 523. Muscle Nerve. 1992. PMID: 1565125 No abstract available.

6

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: hoogendijk je. J Neurol. 1992 May;239(5):277-83. doi: 10.1007/BF00810353. J Neurol. 1992. PMID: 1607892

7

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. Hum Genet. 1991 Dec;88(2):215-8. doi: 10.1007/BF00206075. Hum Genet. 1991. PMID: 1721895

8

[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. Ned Tijdschr Geneeskd. 1991 Dec 21;135(51):2412-4. Ned Tijdschr Geneeskd. 1991. PMID: 1758499 Dutch. No abstract available.

9

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group.

Raeymaekers P, Timmerman V, Nelis E, De Jonghe P, Hoogendijk JE, Baas F, Barker DF, Martin JJ, De Visser M, Bolhuis PA, et al. Raeymaekers P, et al. Among authors: hoogendijk je. Neuromuscul Disord. 1991;1(2):93-7. doi: 10.1016/0960-8966(91)90055-w. Neuromuscul Disord. 1991. PMID: 1822787

10

Calf enlargement in hereditary motor and sensory neuropathy.

De Visser M, Hoogendijk JE, Ongerboer BW, Verbeeten BJ Jr. De Visser M, et al. Among authors: hoogendijk je. Muscle Nerve. 1990 Jan;13(1):40-6. doi: 10.1002/mus.880130109. Muscle Nerve. 1990. PMID: 2325700

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