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Journal of Medical Genetics
|
March 8, 2003
Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism
Y J Crow, D N Black, M Ali, et al.
Urology
|
October 9, 2007
Identification of early p53 mutations in clam ileocystoplasties using restriction site mutation assay
Kenneth D Ivil, Spencer A Jenkins, Shareen H Doak, et al.
Epilepsia
|
April 19, 2003
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy
Ailsa McLellan, Hilary A Phillips, Christopher Rittey, et al.
Neuropediatrics
|
March 6, 2004
Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument
Y J Crow, J McMenamin, C A Haenggeli, et al.
British Journal of Cancer
|
March 21, 2013
Sunitinib in combination with gemcitabine for advanced solid tumours: a phase I dose-finding study
M D Michaelson, A X Zhu, D P Ryan, et al.
Journal of Pediatric Orthopedics
|
February 15, 2023
Femoral Deformity in Tibia Vara and Its Response to Growth Modulation
Janet L Walker, David M Dueber, Allison C Scott, et al.
Journal of Clinical Epidemiology
|
January 1, 1989
Effects on blood pressure of a decrease in sodium use in institutional food preparation: the Exeter-Andover Project
R C Ellison, A L Capper, W P Stephenson, et al.
Journal of Pediatric Orthopedics
|
March 24, 2023
Predicting Success of Deformity Correction With Tension Band Plating in Early-Onset Tibia Vara
Janet L Walker, David M Dueber, Lindsay P Stephenson, et al.
The American Journal of Cardiology
|
March 1, 1991
Expanded clinical evaluation of lovastatin (EXCEL) study results. II. Assessment of the human lens after 48 weeks of treatment with lovastatin
A M Laties, C L Shear, E A Lippa, et al.
Brain : a Journal of Neurology
|
June 4, 1999
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
S M Zuberi, L H Eunson, A Spauschus, et al.
Page
of 25
Search research articles
Search
Showing results (231-240 of 248) with videos related to
Sort By:
Page
of 25
Journal of Medical Genetics
|
March 8, 2003
Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism
Y J Crow, D N Black, M Ali, et al.
Urology
|
October 9, 2007
Identification of early p53 mutations in clam ileocystoplasties using restriction site mutation assay
Kenneth D Ivil, Spencer A Jenkins, Shareen H Doak, et al.
Epilepsia
|
April 19, 2003
Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy
Ailsa McLellan, Hilary A Phillips, Christopher Rittey, et al.
Neuropediatrics
|
March 6, 2004
Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument
Y J Crow, J McMenamin, C A Haenggeli, et al.
British Journal of Cancer
|
March 21, 2013
Sunitinib in combination with gemcitabine for advanced solid tumours: a phase I dose-finding study
M D Michaelson, A X Zhu, D P Ryan, et al.
Journal of Pediatric Orthopedics
|
February 15, 2023
Femoral Deformity in Tibia Vara and Its Response to Growth Modulation
Janet L Walker, David M Dueber, Allison C Scott, et al.
Journal of Clinical Epidemiology
|
January 1, 1989
Effects on blood pressure of a decrease in sodium use in institutional food preparation: the Exeter-Andover Project
R C Ellison, A L Capper, W P Stephenson, et al.
Journal of Pediatric Orthopedics
|
March 24, 2023
Predicting Success of Deformity Correction With Tension Band Plating in Early-Onset Tibia Vara
Janet L Walker, David M Dueber, Lindsay P Stephenson, et al.
The American Journal of Cardiology
|
March 1, 1991
Expanded clinical evaluation of lovastatin (EXCEL) study results. II. Assessment of the human lens after 48 weeks of treatment with lovastatin
A M Laties, C L Shear, E A Lippa, et al.
Brain : a Journal of Neurology
|
June 4, 1999
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
S M Zuberi, L H Eunson, A Spauschus, et al.
Page
of 25