Lammens M - Search Results

1

Myopathy and polyneuropathy in an adolescent with the kyphoscoliotic type of Ehlers-Danlos syndrome.

Voermans NC, Bönnemann CG, Lammens M, van Engelen BG, Hamel BC. Voermans NC, et al. Among authors: lammens m. Am J Med Genet A. 2009 Oct;149A(10):2311-6. doi: 10.1002/ajmg.a.32997. Am J Med Genet A. 2009. PMID: 19760654 No abstract available.

2

Mononeuropathy multiplex as the initial manifestation of neurofibromatosis type 2.

Gijtenbeek JM, Gabreëls-Festen AA, Lammens M, Zwarts MJ, van Engelen BG. Gijtenbeek JM, et al. Among authors: lammens m. Neurology. 2001 Jun 26;56(12):1766-8. doi: 10.1212/wnl.56.12.1766. Neurology. 2001. PMID: 11425952

3

A new phenotype of autosomal dominant nemaline myopathy.

Gommans IM, van Engelen BG, ter Laak HJ, Brunner HG, Kremer H, Lammens M, Vogels OJ. Gommans IM, et al. Among authors: lammens m. Neuromuscul Disord. 2002 Jan;12(1):13-8. doi: 10.1016/s0960-8966(01)00231-0. Neuromuscul Disord. 2002. PMID: 11731279

4

MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings.

Geerdink N, Rotteveel JJ, Lammens M, Sistermans EA, Heikens GT, Gabreëls FJ, Mullaart RA, Hamel BC. Geerdink N, et al. Among authors: lammens m. Neuropediatrics. 2002 Feb;33(1):33-6. doi: 10.1055/s-2002-23598. Neuropediatrics. 2002. PMID: 11930274

5

A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions.

Gommans IM, Davis M, Saar K, Lammens M, Mastaglia F, Lamont P, van Duijnhoven G, ter Laak HJ, Reis A, Vogels OJ, Laing N, van Engelen BG, Kremer H. Gommans IM, et al. Among authors: lammens m. Brain. 2003 Jul;126(Pt 7):1545-51. doi: 10.1093/brain/awg162. Epub 2003 Jun 4. Brain. 2003. PMID: 12805120

6

Nijmegen breakage syndrome: a neuropathological study.

Lammens M, Hiel JA, Gabreëls FJ, van Engelen BG, van den Heuvel LP, Weemaes CM. Lammens M, et al. Neuropediatrics. 2003 Aug;34(4):189-93. doi: 10.1055/s-2003-42207. Neuropediatrics. 2003. PMID: 12973659

7

The lethal phenotype of a homozygous nonsense mutation in the lamin A/C gene.

van Engelen BG, Muchir A, Hutchison CJ, van der Kooi AJ, Bonne G, Lammens M. van Engelen BG, et al. Among authors: lammens m. Neurology. 2005 Jan 25;64(2):374-6. doi: 10.1212/01.WNL.0000149763.15180.00. Neurology. 2005. PMID: 15668447

8

Statin-disclosed acid maltase deficiency.

Voermans NC, Lammens M, Wevers RA, Hermus AR, van Engelen BG. Voermans NC, et al. Among authors: lammens m. J Intern Med. 2005 Aug;258(2):196-7. doi: 10.1111/j.1365-2796.2005.01515.x. J Intern Med. 2005. PMID: 16018797 Free article. No abstract available.

9

Recurrent neuropathy associated with Ehlers-Danlos syndrome.

Voermans NC, Drost G, van Kampen A, Gabreëls-Festen AA, Lammens M, Hamel BC, Schalkwijk J, van Engelen BG. Voermans NC, et al. Among authors: lammens m. J Neurol. 2006 May;253(5):670-1. doi: 10.1007/s00415-005-0056-0. Epub 2005 Nov 29. J Neurol. 2006. PMID: 16311893 No abstract available.

10

Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia.

Hiel JA, van Engelen BG, Weemaes CM, Broeks A, Verrips A, ter Laak H, Vingerhoets HM, van den Heuvel LP, Lammens M, Gabreëls FJ, Last JI, Taylor AM. Hiel JA, et al. Among authors: lammens m. Neurology. 2006 Jul 25;67(2):346-9. doi: 10.1212/01.wnl.0000224878.22821.23. Neurology. 2006. PMID: 16864838

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