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The Journal of Pediatrics|July 1, 1991
Hypercalciuria in children severely affected with osteogenesis imperfectaA Chines, D J Petersen, F W Schranck, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 1992
X-linked hypophosphatemic rickets: a study (with literature review) of linear growth response to calcitriol and phosphate therapyD J Petersen, A M Boniface, F W Schranck, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1996
X-linked hypophosphatemia: a search for gender, race, anticipation, or parent of origin effects on disease expression in childrenM P Whyte, F W Schranck, R Armamento-Villareal
American Journal of Medical Genetics|July 1, 1990
Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndromeM P Whyte, D J Petersen, W H McAlister
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 1, 1996
Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disordersM P Whyte, A Chines, D P Silva, et al.
Calcified Tissue International|March 14, 1998
Differing lumbar vertebral mineralization rates in ambulatory pediatric patients with osteogenesis imperfectaW R Reinus, W H McAlister, F Schranck, et al.
The American Journal of Medicine|September 1, 1992
Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemiaC T McMurtry, F W Schranck, D A Walkenhorst, et al.
Clinical Orthopaedics and Related Research|September 1, 1993
Carbonic anhydrase II deficiencyM P Whyte
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