Van den Bergh P - Search Results

1

Mutations in SACS cause atypical and late-onset forms of ARSACS.

Baets J, Deconinck T, Smets K, Goossens D, Van den Bergh P, Dahan K, Schmedding E, Santens P, Rasic VM, Van Damme P, Robberecht W, De Meirleir L, Michielsens B, Del-Favero J, Jordanova A, De Jonghe P. Baets J, et al. Among authors: van damme p, van den bergh p. Neurology. 2010 Sep 28;75(13):1181-8. doi: 10.1212/WNL.0b013e3181f4d86c. Neurology. 2010. PMID: 20876471

2

Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures.

Vanherpe P, Fieuws S, D'Hondt A, Bleyenheuft C, Demaerel P, De Bleecker J, Van den Bergh P, Baets J, Remiche G, Verhoeven K, Delstanche S, Toussaint M, Buyse B, Van Damme P, Depuydt CE, Claeys KG. Vanherpe P, et al. Among authors: van damme p, van den bergh p. Orphanet J Rare Dis. 2020 Apr 5;15(1):83. doi: 10.1186/s13023-020-01353-4. Orphanet J Rare Dis. 2020. PMID: 32248831 Free PMC article.

3

Early stages of building a rare disease registry, methods and 2010 data from the Belgian Neuromuscular Disease Registry (BNMDR).

Roy AJ, Van den Bergh P, Van Damme P, Doggen K, Van Casteren V; BNMDR Scientific Committee. Roy AJ, et al. Among authors: van casteren v, van damme p, van den bergh p. Acta Neurol Belg. 2015 Jun;115(2):97-104. doi: 10.1007/s13760-014-0320-0. Epub 2014 Jun 24. Acta Neurol Belg. 2015. PMID: 24957677 Free PMC article.

4

Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease.

Van den Bergh PY, Gérard JM, Elosegi JA, Manto MU, Kubisch C, Schoser BG. Van den Bergh PY, et al. J Neurol Neurosurg Psychiatry. 2004 Sep;75(9):1349-51. doi: 10.1136/jnnp.2003.028217. J Neurol Neurosurg Psychiatry. 2004. PMID: 15314133 Free PMC article.

5

Dose standardization of botulinum toxin.

Van den Bergh PY, Lison DF. Van den Bergh PY, et al. Adv Neurol. 1998;78:231-5. Adv Neurol. 1998. PMID: 9750920 No abstract available.

6

Somatosensory evoked potentials and jerk-locked EEG back-averaging in myoclonic epilepsy.

Guérit JM, Van den Bergh P, Gobiet Y, Laterre EC. Guérit JM, et al. Among authors: van den bergh p. Eur Neurol. 1994;34 Suppl 1:49-54. doi: 10.1159/000119509. Eur Neurol. 1994. PMID: 8001610

7

Necrotizing myopathy with microvascular deposition of the complement membrane attack complex.

De Bleecker J, Vervaet V, Van den Bergh P. De Bleecker J, et al. Among authors: van den bergh p. Clin Neuropathol. 2004 Mar-Apr;23(2):76-9. Clin Neuropathol. 2004. PMID: 15074581

8

International Symposium on Neuromuscular Disorders state-of-the-art at the edge of the millennium Brussels, December 11th, 1999.

Van den Bergh PY. Van den Bergh PY. Acta Neurol Belg. 2000 Sep;100(3):141. Acta Neurol Belg. 2000. PMID: 11098284 No abstract available.

9

Paraneoplastic rhombencephalitis and brachial plexopathy in two cases of amphiphysin auto-immunity.

Coppens T, Van den Bergh P, Duprez TJ, Jeanjean A, De Ridder F, Sindic CJ. Coppens T, et al. Among authors: van den bergh p. Eur Neurol. 2006;55(2):80-3. doi: 10.1159/000092307. Epub 2006 Mar 24. Eur Neurol. 2006. PMID: 16567945

10

Peroneal nerve palsy in anorexia nervosa.

Lutte I, Rhys C, Hubert C, Brion F, Boland B, Peeters A, Van Den Bergh P, Lambert M. Lutte I, et al. Among authors: van den bergh p. Acta Neurol Belg. 1997 Dec;97(4):251-4. Acta Neurol Belg. 1997. PMID: 9478264 Review.

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