Whyte MP - Search Results

1

COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta.

Lindahl K, Barnes AM, Fratzl-Zelman N, Whyte MP, Hefferan TE, Makareeva E, Brusel M, Yaszemski MJ, Rubin CJ, Kindmark A, Roschger P, Klaushofer K, McAlister WH, Mumm S, Leikin S, Kessler E, Boskey AL, Ljunggren O, Marini JC. Lindahl K, et al. Among authors: whyte mp. Hum Mutat. 2011 Jun;32(6):598-609. doi: 10.1002/humu.21475. Epub 2011 Apr 7. Hum Mutat. 2011. PMID: 21344539 Free PMC article.

2

Occipital horn syndrome. Additional radiographic findings in two new cases.

Herman TE, McAlister WH, Boniface A, Whyte MP. Herman TE, et al. Among authors: whyte mp. Pediatr Radiol. 1992;22(5):363-5. doi: 10.1007/BF02016258. Pediatr Radiol. 1992. PMID: 1408447

3

Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.

Whyte MP, Petersen DJ, McAlister WH. Whyte MP, et al. Am J Med Genet. 1990 Jul;36(3):288-91. doi: 10.1002/ajmg.1320360308. Am J Med Genet. 1990. PMID: 2363424

4

Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literature.

Civitelli R, McAlister WH, Teitelbaum SL, Whyte MP. Civitelli R, et al. Among authors: whyte mp. J Bone Miner Res. 1989 Dec;4(6):863-75. doi: 10.1002/jbmr.5650040611. J Bone Miner Res. 1989. PMID: 2692405 Review.

5

Tibial bowing exacerbated by partial premature epiphyseal closure in sex-linked hypophosphatemic rickets.

McAlister WH, Kim GS, Whyte MP. McAlister WH, et al. Among authors: whyte mp. Radiology. 1987 Feb;162(2):461-3. doi: 10.1148/radiology.162.2.3025921. Radiology. 1987. PMID: 3025921

6

Macroepiphyseal dysplasia with symptomatic osteoporosis, wrinkled skin, and aged appearance: a presumed autosomal recessive condition.

McAlister WH, Coe JD, Whyte MP. McAlister WH, et al. Among authors: whyte mp. Skeletal Radiol. 1986;15(1):47-51. doi: 10.1007/BF00355073. Skeletal Radiol. 1986. PMID: 3941923

7

Intermittent radiographic changes of rickets without defective trabecular bone mineralization in a case of spondylometaphyseal dysplasia.

Kim GS, McAlister WH, Whyte MP. Kim GS, et al. Among authors: whyte mp. Bone. 1986;7(1):1-7. doi: 10.1016/8756-3282(86)90144-4. Bone. 1986. PMID: 3964492

8

Hypercalciuria in osteogenesis imperfecta: a follow-up study to assess renal effects.

Chines A, Boniface A, McAlister W, Whyte M. Chines A, et al. Bone. 1995 Mar;16(3):333-9. doi: 10.1016/8756-3282(94)00046-8. Bone. 1995. PMID: 7786636

9

Spondyloepimetaphyseal dysplasia: clinical and radiologic investigation of a large kindred manifesting autosomal dominant inheritance, and a review of the literature.

Patel AC, McAlister WH, Whyte MP. Patel AC, et al. Among authors: whyte mp. Medicine (Baltimore). 1993 Sep;72(5):326-42. Medicine (Baltimore). 1993. PMID: 8412645 Review.

10

Differing lumbar vertebral mineralization rates in ambulatory pediatric patients with osteogenesis imperfecta.

Reinus WR, McAlister WH, Schranck F, Chines A, Whyte MP. Reinus WR, et al. Among authors: whyte mp. Calcif Tissue Int. 1998 Jan;62(1):17-20. doi: 10.1007/s002239900387. Calcif Tissue Int. 1998. PMID: 9405727

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