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C E Jackson

Showing results (141-150 of 180) with videos related to

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Surgery|July 6, 2000
Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutationG L Feldman, M W Edmonds, P J Ainsworth, et al.
Muscle & Nerve|May 20, 1999
Multifocal acquired demyelinating sensory and motor neuropathy: the Lewis-Sumner syndromeD S Saperstein, A A Amato, G I Wolfe, et al.
Anesthesiology|March 1, 1988
Epidural sufentanil for postoperative analgesia after cesarean sectionM A Rosen, P A Dailey, S C Hughes, et al.
The Journal of Pediatrics|November 20, 1998
The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosisA J Infante, H A Britton, T DeNapoli, et al.
American Journal of Human Genetics|July 1, 1997
The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2J N Berg, C J Gallione, T T Stenzel, et al.
Nature|August 6, 1987
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkageN E Simpson, K K Kidd, P J Goodfellow, et al.
Human Molecular Genetics|February 1, 1994
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumoursC Eng, D P Smith, L M Mulligan, et al.
Archives of Neurology|February 1, 1994
Immunosuppressive treatment of motor neuron syndromes. Attempts to distinguish a treatable disorderE Tan, D J Lynn, A A Amato, et al.
American Journal of Human Genetics|December 5, 1998
Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31H Feit, A Silbergleit, L B Schneider, et al.
Journal of the Neurological Sciences|October 26, 2001
A preliminary evaluation of a prospective study of pulmonary function studies and symptoms of hypoventilation in ALS/MND patientsC E Jackson, J Rosenfeld, D H Moore, et al.
Pageof 18

Showing results (141-150 of 180) with videos related to

Sort By:
Pageof 18
Surgery|July 6, 2000
Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutationG L Feldman, M W Edmonds, P J Ainsworth, et al.
Muscle & Nerve|May 20, 1999
Multifocal acquired demyelinating sensory and motor neuropathy: the Lewis-Sumner syndromeD S Saperstein, A A Amato, G I Wolfe, et al.
Anesthesiology|March 1, 1988
Epidural sufentanil for postoperative analgesia after cesarean sectionM A Rosen, P A Dailey, S C Hughes, et al.
The Journal of Pediatrics|November 20, 1998
The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosisA J Infante, H A Britton, T DeNapoli, et al.
American Journal of Human Genetics|July 1, 1997
The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2J N Berg, C J Gallione, T T Stenzel, et al.
Nature|August 6, 1987
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkageN E Simpson, K K Kidd, P J Goodfellow, et al.
Human Molecular Genetics|February 1, 1994
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumoursC Eng, D P Smith, L M Mulligan, et al.
Archives of Neurology|February 1, 1994
Immunosuppressive treatment of motor neuron syndromes. Attempts to distinguish a treatable disorderE Tan, D J Lynn, A A Amato, et al.
American Journal of Human Genetics|December 5, 1998
Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31H Feit, A Silbergleit, L B Schneider, et al.
Journal of the Neurological Sciences|October 26, 2001
A preliminary evaluation of a prospective study of pulmonary function studies and symptoms of hypoventilation in ALS/MND patientsC E Jackson, J Rosenfeld, D H Moore, et al.
Pageof 18