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Items: 5

1.

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

Maystadt I, Zarhrate M, Leclair-Richard D, Estournet B, Barois A, Renault F, Routon MC, Durand MC, Lefebvre S, Munnich A, Verellen-Dumoulin C, Viollet L.

Neurology. 2006 Jul 11;67(1):120-4. Epub 2006 May 25.

PMID:
16728649
2.

[Spinal muscular atrophy. A 4-year prospective, multicenter, longitudinal study (168 cases)].

Barois A, Mayer M, Desguerre I, Chabrol B, Berard C, Cuisset JM, Leclair-Richard D, Visconti-Lougovoy J, Hatton F, Estournet-Mathiaud B.

Bull Acad Natl Med. 2005 Jun;189(6):1181-98; discussion 1198-9. French.

PMID:
16433443
3.

Respiratory capacity course in patients with infantile spinal muscular atrophy.

Ioos C, Leclair-Richard D, Mrad S, Barois A, Estournet-Mathiaud B.

Chest. 2004 Sep;126(3):831-7.

PMID:
15364763
4.

[Neuromuscular diseases. The everyday admission of patients].

Leclair-Richard D, Paumier B.

Soins Gynecol Obstet Pueric Pediatr. 1993 Dec-1994 Jan;(151-152):12-4. French. No abstract available.

PMID:
8009372
5.

[Infantile spinal muscular atrophy].

Barois A, Estournet B, Duval-Beaupère G, Bataille J, Leclair-Richard D.

Rev Neurol (Paris). 1989;145(4):299-304. French.

PMID:
2660222

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