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M P Whyte

Showing results (61-70 of 166) with videos related to

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Gene|October 12, 2001
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice siteS Mumm, X Zhang, M Vacca, et al.
The Journal of Pediatrics|July 1, 1991
Hypercalciuria in children severely affected with osteogenesis imperfectaA Chines, D J Petersen, F W Schranck, et al.
Calcified Tissue International|March 1, 1986
Mixed-sclerosing-bone-dystrophy: 42-year follow-up of a case reported as osteopetrosisR Pacifici, W A Murphy, S L Teitelbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1989
Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literatureR Civitelli, W H McAlister, S L Teitelbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 1, 1996
Absence of paramyxo virus transcripts in juvenile Paget bone diseaseM P Whyte, R Leelawattana, S V Reddy, et al.
Pediatric Radiology|January 1, 1992
Occipital horn syndrome. Additional radiographic findings in two new casesT E Herman, W H McAlister, A Boniface, et al.
The Journal of Pediatrics|September 1, 1982
Infantile hypophosphatasia: enzyme replacement therapy by intravenous infusion of alkaline phosphatase-rich plasma from patients with Paget bone diseaseM P Whyte, R Valdes, L M Ryan, et al.
The American Journal of Medicine|August 1, 1987
Hypercalcemic hyperparathyroidism complicating oncogenic osteomalacia. Effect of successful tumor resection on mineral homeostasisI R Reid, S L Teitelbaum, A Dusso, et al.
American Journal of Ophthalmology|April 15, 1985
Failure of acetazolamide to decrease intraocular pressure in patients with carbonic anhydrase II deficiencyT Krupin, W S Sly, M P Whyte, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 29, 2000
"Café-au-lait spots" caused by vitiligo in McCune-Albright syndromeM P Whyte, M N Podgornik, J Zerega, et al.
Pageof 17

Showing results (61-70 of 166) with videos related to

Sort By:
Pageof 17
Gene|October 12, 2001
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice siteS Mumm, X Zhang, M Vacca, et al.
The Journal of Pediatrics|July 1, 1991
Hypercalciuria in children severely affected with osteogenesis imperfectaA Chines, D J Petersen, F W Schranck, et al.
Calcified Tissue International|March 1, 1986
Mixed-sclerosing-bone-dystrophy: 42-year follow-up of a case reported as osteopetrosisR Pacifici, W A Murphy, S L Teitelbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1989
Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literatureR Civitelli, W H McAlister, S L Teitelbaum, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 1, 1996
Absence of paramyxo virus transcripts in juvenile Paget bone diseaseM P Whyte, R Leelawattana, S V Reddy, et al.
Pediatric Radiology|January 1, 1992
Occipital horn syndrome. Additional radiographic findings in two new casesT E Herman, W H McAlister, A Boniface, et al.
The Journal of Pediatrics|September 1, 1982
Infantile hypophosphatasia: enzyme replacement therapy by intravenous infusion of alkaline phosphatase-rich plasma from patients with Paget bone diseaseM P Whyte, R Valdes, L M Ryan, et al.
The American Journal of Medicine|August 1, 1987
Hypercalcemic hyperparathyroidism complicating oncogenic osteomalacia. Effect of successful tumor resection on mineral homeostasisI R Reid, S L Teitelbaum, A Dusso, et al.
American Journal of Ophthalmology|April 15, 1985
Failure of acetazolamide to decrease intraocular pressure in patients with carbonic anhydrase II deficiencyT Krupin, W S Sly, M P Whyte, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 29, 2000
"Café-au-lait spots" caused by vitiligo in McCune-Albright syndromeM P Whyte, M N Podgornik, J Zerega, et al.
Pageof 17