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E Emery

Showing results (111-120 of 425) with videos related to

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Advances in Neurology|January 1, 1982
Familial motor neuron diseasesA E Emery, S Holloway
British Medical Journal|February 9, 1980
Intracellular calcium and pathogenesis and antenatal diagnosis of Duchenne muscular dystrophyA E Emery, D Burt
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1972
Amino acid, creatine and creatinine studies in myotonic dystrophyA E Emery, D Burt
Journal of the Neurological Sciences|November 1, 1973
Leucocyte fatty acid oxidation in hereditary neuromuscular disorders. A preliminary reportB King, A E Emery
Clinical Genetics|January 1, 1971
Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease)K Fried, A E Emery
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 14, 1982
Antenatal diagnosis--its present status and future prospectsA E Emery, P Beighton
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 24, 1981
Erythrocyte spectrin in Duchenne muscular dystrophyR Anand, A E Emery
Journal of the American Academy of Child and Adolescent Psychiatry|March 1, 1988
Chronic family adversity and school-age children's adjustmentD S Shaw, R E Emery
Neuromuscular Disorders : NMD|September 21, 2000
Lockhart Clarke (1817-1880): his role in the early history of muscular dystrophyA E Emery, M L Emery
Lancet (London, England)|April 7, 1973
Arginine-glycine amidinotransferase activity in myotonic dystrophyC E Bolton, A E Emery
Pageof 43

Showing results (111-120 of 425) with videos related to

Sort By:
Pageof 43
Advances in Neurology|January 1, 1982
Familial motor neuron diseasesA E Emery, S Holloway
British Medical Journal|February 9, 1980
Intracellular calcium and pathogenesis and antenatal diagnosis of Duchenne muscular dystrophyA E Emery, D Burt
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 1, 1972
Amino acid, creatine and creatinine studies in myotonic dystrophyA E Emery, D Burt
Journal of the Neurological Sciences|November 1, 1973
Leucocyte fatty acid oxidation in hereditary neuromuscular disorders. A preliminary reportB King, A E Emery
Clinical Genetics|January 1, 1971
Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease)K Fried, A E Emery
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 14, 1982
Antenatal diagnosis--its present status and future prospectsA E Emery, P Beighton
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 24, 1981
Erythrocyte spectrin in Duchenne muscular dystrophyR Anand, A E Emery
Journal of the American Academy of Child and Adolescent Psychiatry|March 1, 1988
Chronic family adversity and school-age children's adjustmentD S Shaw, R E Emery
Neuromuscular Disorders : NMD|September 21, 2000
Lockhart Clarke (1817-1880): his role in the early history of muscular dystrophyA E Emery, M L Emery
Lancet (London, England)|April 7, 1973
Arginine-glycine amidinotransferase activity in myotonic dystrophyC E Bolton, A E Emery
Pageof 43