Gabreels FJ - Search Results

1

Are muscle cramps in Isaacs' syndrome triggered by human immunoglobulin?

Van Engelen BG, Benders AA, Gabreels FJ, Veerkamp JH. Van Engelen BG, et al. Among authors: gabreels fj. J Neurol Neurosurg Psychiatry. 1995 Mar;58(3):393. doi: 10.1136/jnnp.58.3.393. J Neurol Neurosurg Psychiatry. 1995. PMID: 7755748 Free PMC article. No abstract available.

2

Immunoglobulin treatment in epilepsy, a review of the literature.

van Engelen BG, Renier WO, Weemaes CM, Gabreels FJ, Meinardi H. van Engelen BG, et al. Among authors: gabreels fj. Epilepsy Res. 1994 Dec;19(3):181-90. doi: 10.1016/0920-1211(94)90061-2. Epilepsy Res. 1994. PMID: 7698094 Review.

3

Congenital fibre type disproportion a time-locked diagnosis: a clinical and morphological follow-up study.

Bartholomeus MG, Gabreëls FJ, ter Laak HJ, van Engelen BG. Bartholomeus MG, et al. Among authors: gabreels fj. Clin Neurol Neurosurg. 2000 Jun;102(2):97-101. doi: 10.1016/s0303-8467(00)00066-4. Clin Neurol Neurosurg. 2000. PMID: 10817896 Review.

4

Histology of hereditary neuralgic amyotrophy.

van Alfen N, Gabreëls-Festen AA, Ter Laak HJ, Arts WF, Gabreëls FJ, van Engelen BG. van Alfen N, et al. Among authors: gabreels fj. J Neurol Neurosurg Psychiatry. 2005 Mar;76(3):445-7. doi: 10.1136/jnnp.2004.044370. J Neurol Neurosurg Psychiatry. 2005. PMID: 15716548 Free PMC article.

5

Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.

Gabreëls-Festen A, van Beersum S, Eshuis L, LeGuern E, Gabreëls F, van Engelen B, Mariman E. Gabreëls-Festen A, et al. J Neurol Neurosurg Psychiatry. 1999 May;66(5):569-74. doi: 10.1136/jnnp.66.5.569. J Neurol Neurosurg Psychiatry. 1999. PMID: 10209165 Free PMC article.

6

Intravenous immunoglobulin preparation increases myoplasmic calcium concentration by activating the dihydropyridine-ryanodine receptor complex.

van Engelen BG, Benders AA, Wevers RA, Gabreëls FJ, Renier WO, Veerkamp JH. van Engelen BG, et al. Among authors: gabreels fj. J Neurol Sci. 1998;156(1):35-40. doi: 10.1016/s0022-510x(98)00022-7. J Neurol Sci. 1998. PMID: 9559984

7

A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.

de Vries DD, van Engelen BG, Gabreëls FJ, Ruitenbeek W, van Oost BA. de Vries DD, et al. Among authors: gabreels fj. Ann Neurol. 1993 Sep;34(3):410-2. doi: 10.1002/ana.410340319. Ann Neurol. 1993. PMID: 8395787

8

Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease.

Gabreëls-Festen AA, Hoogendijk JE, Meijerink PH, Gabreëls FJ, Bolhuis PA, van Beersum S, Kulkens T, Nelis E, Jennekens FG, de Visser M, van Engelen BG, Van Broeckhoven C, Mariman EC. Gabreëls-Festen AA, et al. Among authors: gabreels fj. Neurology. 1996 Sep;47(3):761-5. doi: 10.1212/wnl.47.3.761. Neurology. 1996. PMID: 8797476

9

Diagnosis and differential diagnosis of muscle cramps: a clinical approach.

Jansen PH, Gabreëls FJ, van Engelen BG. Jansen PH, et al. Among authors: gabreels fj. J Clin Neuromuscul Dis. 2002 Dec;4(2):89-94. doi: 10.1097/00131402-200212000-00008. J Clin Neuromuscul Dis. 2002. PMID: 19078696

10

Cerebrospinal fluid examinations in cryptogenic West and Lennox-Gastaut syndrome before and after intravenous immunoglobulin administration.

van Engelen BG, Renier WO, Weemaes CM, Lamers KJ, Gabreels FJ, Meinardi H. van Engelen BG, et al. Among authors: gabreels fj. Epilepsy Res. 1994 Jun;18(2):139-47. doi: 10.1016/0920-1211(94)90006-x. Epilepsy Res. 1994. PMID: 7957036 Clinical Trial.

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