Gabreëls-Festen AA - Search Results

1

Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.

Gabreëls-Festen AA, Gabreëls FJ, Hoogendijk JE, Bolhuis PA, Jongen PJ, Vingerhoets HM. Gabreëls-Festen AA, et al. Acta Neuropathol. 1993;86(6):630-5. doi: 10.1007/BF00294303. Acta Neuropathol. 1993. PMID: 8310819

2

Hereditary neuropathy with liability to pressure palsies in childhood.

Gabreëls-Festen AA, Gabreëls FJ, Joosten EM, Vingerhoets HM, Renier WO. Gabreëls-Festen AA, et al. Neuropediatrics. 1992 Jun;23(3):138-43. doi: 10.1055/s-2008-1071329. Neuropediatrics. 1992. PMID: 1322507

3

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

4

Autosomal recessive form of hereditary motor and sensory neuropathy type I.

Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Joosten EM, Janssen-van Kempen TW. Gabreëls-Festen AA, et al. Neurology. 1992 Sep;42(9):1755-61. doi: 10.1212/wnl.42.9.1755. Neurology. 1992. PMID: 1513466

5

Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I).

Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW. Gabreëls-Festen AA, et al. J Neurol Sci. 1992 Feb;107(2):145-54. doi: 10.1016/0022-510x(92)90282-p. J Neurol Sci. 1992. PMID: 1564512

6

Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.

Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Gooskens RH, Stegeman DF. Gabreëls-Festen AA, et al. Brain. 1991 Aug;114 ( Pt 4):1855-70. doi: 10.1093/brain/114.4.1855. Brain. 1991. PMID: 1884182

7

Polyglucosan bodies in sural nerve biopsies.

Busard HL, Gabreëls-Festen AA, van 't Hof MA, Renier WO, Gabreëls FJ. Busard HL, et al. Acta Neuropathol. 1990;80(5):554-7. doi: 10.1007/BF00294618. Acta Neuropathol. 1990. PMID: 2251913

8

Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.

Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Stegeman DF, Vos AJ, Busch HF. Gabreëls-Festen AA, et al. Brain. 1990 Dec;113 ( Pt 6):1629-43. doi: 10.1093/brain/113.6.1629. Brain. 1990. PMID: 2276038

9

Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies.

Mariman EC, Gabreëls-Festen AA, van Beersum SE, Jongen PJ, van de Looij E, Baas F, Bolhuis PA, Ropers HH, Gabreëls FJ. Mariman EC, et al. Hum Genet. 1994 Feb;93(2):151-6. doi: 10.1007/BF00210601. Hum Genet. 1994. PMID: 8112739

10

The status of HMSN type III.

Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW. Gabreëls-Festen AA, et al. Neuromuscul Disord. 1994 Jan;4(1):63-9. doi: 10.1016/0960-8966(94)90049-3. Neuromuscul Disord. 1994. PMID: 8173353

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