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Academic Journal

Enuresis and urinary incontinence in children and adolescents with spinal muscular atrophy.

Authors : Von Gontard, A.¹; Laufersweiler-Plass, C.¹; Backes, M.¹

Source: BJU International. Sep2001, Vol. 88 Issue 4, p409-413. 5p. 2 Charts.

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Academic Journal

Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy.

Authors : Bodine, Sue C.; Latres, Esther; Baumhueter, Susanne

Source: Science. 11/23/2001, Vol. 294 Issue 5547, p1704-1708. 5p. 3 Color Photographs, 9 Black and White Photographs, 2 Graphs.

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Academic Journal

Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein.

Authors : Gangwani, Laxman; Mikrut, Monique; Theroux, Steven

Source: Nature Cell Biology. Apr2001, Vol. 3 Issue 4, p376. 8p.

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Academic Journal

Gene Deletion Patterns in Spinal Muscular Atrophy Patients with Different Clinical Phenotypes.

Authors : Haider¹; Moosa¹; Dalal¹

Source: Journal of Biomedical Science. 2001, Vol. 8 Issue 2, p191-196. 6p. 2 Black and White Photographs, 2 Charts.

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Academic Journal

Validity of the EK scale: a functional assessment of non-ambulatory individuals with Duchenne muscular dystrophy or spinal muscular atrophy.

Authors : Steffensen, Birgit; Hyde, Sylvia; Lyager, Soren

Source: Physiotherapy Research International. Sep2001, Vol. 6 Issue 3, p119. 16p. 3 Charts, 1 Graph.

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Academic Journal

Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world.

Authors : Lund, Annastiina; Udd, Bjarne; Juvonen, Vesa

Source: European Journal of Human Genetics. Jun2001, Vol. 9 Issue 6, p431. 6p.

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Academic Journal

On the possible role of muscle in the pathogenesis of spinal muscular atrophy.

Authors : Guettier-Sigrist, Séverine; Coupin, Gilliane; Braun, Serge

Source: Fundamental & Clinical Pharmacology. Feb2001, Vol. 15 Issue 1, p31. 10p. 17 Black and White Photographs, 2 Diagrams, 1 Chart, 6 Graphs.

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Academic Journal

Best practice guidelines for molecular analysis in spinal muscular atrophy.

Authors : Scheffer, Hans; Cobben, Jan Maarten; Matthijs, Gert

Source: European Journal of Human Genetics. Jul2001, Vol. 9 Issue 7, p484. 8p.

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Academic Journal

Juvenile asymmetric segmental spinal muscular atrophy (Hirayama's disease) Three cases without evidence of “flexion myelopathy”.

Authors : Willeit, J.¹; Kiechl, S.¹; Kiechl-Kohlendorfer, U.²

Source: Acta Neurologica Scandinavica. Nov2001, Vol. 104 Issue 5, p320-322. 3p. 4 Black and White Photographs.

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Academic Journal

Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1.

Authors : Grohmann, Katja; Schuelke, Markus; Diers, Alexander

Source: Nature Genetics. Sep2001, Vol. 29 Issue 1, p75. 3p.

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فلترة النتائج

Enuresis and urinary incontinence in children and adolescents with spinal muscular atrophy.

Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy.

Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein.

Gene Deletion Patterns in Spinal Muscular Atrophy Patients with Different Clinical Phenotypes.

Validity of the EK scale: a functional assessment of non-ambulatory individuals with Duchenne muscular dystrophy or spinal muscular atrophy.

Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world.

On the possible role of muscle in the pathogenesis of spinal muscular atrophy.

Best practice guidelines for molecular analysis in spinal muscular atrophy.

Juvenile asymmetric segmental spinal muscular atrophy (Hirayama's disease) Three cases without evidence of “flexion myelopathy”.

Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1.

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