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Results:
1-24
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Results: 24
Authors:
Mumm, S
Jones, J
Finnegan, P
Whyte, MP
Citation: S. Mumm et al., Hypophosphatasia: Molecular diagnosis of Rathbun's original case, J BONE MIN, 16(9), 2001, pp. 1724-1727
Authors:
Whyte, MP
Podgornik, MN
Wollberg, VA
Eddy, MC
McAlister, WH
Citation: Mp. Whyte et al., Pseudo-(tumor-induced) rickets, J BONE MIN, 16(8), 2001, pp. 1564-1571
Authors:
Mumm, S
Zhang, XF
Gottesman, GS
McAlister, WH
Whyte, MP
Citation: S. Mumm et al., Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin, J BONE MIN, 16(12), 2001, pp. 2245-2250
Authors:
Mumm, S
Zhang, XF
Vacca, M
D'Esposito, M
Whyte, MP
Citation: S. Mumm et al., The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site, GENE, 273(2), 2001, pp. 285-293
Authors:
Christie, PT
Harding, B
Nesbit, MA
Whyte, MP
Thakker, RV
Citation: Pt. Christie et al., X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene, J CLIN END, 86(8), 2001, pp. 3840-3844
Authors:
Hughes, AE
Ralston, SH
Marken, J
Bell, C
MacPherson, H
Wallace, RGH
van Hul, W
Whyte, MP
Nakatsuka, K
Hovy, L
Anderson, DM
Citation: Ae. Hughes et al., Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis, NAT GENET, 24(1), 2000, pp. 45-48
Authors:
Junge, RE
Gannon, FH
Porton, I
McAlister, WH
Whyte, MP
Citation: Re. Junge et al., Management and prevention of vitamin D deficiency rickets in captive-born juvenile chimpanzees (Pan troglodytes), J ZOO WILD, 31(3), 2000, pp. 361-369
Authors:
Whyte, MP
Eddy, MC
Podgornik, MN
McAlister, WH
Citation: Mp. Whyte et al., Polycystic bone disease, J BONE MIN, 15(2), 2000, pp. 373-373
Authors:
Whyte, MP
Mills, BG
Reinus, WR
Podgornik, MN
Roodman, GD
Gannon, FH
Eddy, MC
McAlister, WH
Citation: Mp. Whyte et al., Expansile skeletal hyperphosphatasia: A new familial metabolic bone disease, J BONE MIN, 15(12), 2000, pp. 2330-2344
Authors:
Whyte, MP
Podgornik, MN
Zerega, J
Reinus, WR
Citation: Mp. Whyte et al., "Cafe-Au-Lait spots" caused by vitiligo in McCune-Albright syndrome, J BONE MIN, 15(12), 2000, pp. 2521-2523
Authors:
Eddy, MC
De Beur, SMJ
Yandow, SM
McAlister, WH
Shore, EM
Kaplan, FS
Whyte, MP
Levine, MA
Citation: Mc. Eddy et al., Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification, J BONE MIN, 15(11), 2000, pp. 2074-2083
Authors:
Steiner, RD
Whyte, MP
Chang, E
Hanks, J
Mattes, C
Senephansiri, H
Gibson, KM
Citation: Rd. Steiner et al., Increased urine heparan and chondroitin sulphate excretion in patients with osteopetrosis, J INH MET D, 23(1), 2000, pp. 88-90
Authors:
Mumm, S
Christie, PT
Finnegan, P
Jones, J
Dixon, PH
Pannett, AAJ
Harding, B
Gottesman, GS
Thakker, RV
Whyte, MP
Citation: S. Mumm et al., A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred, J CLIN END, 85(9), 2000, pp. 3343-3347
Authors:
Whyte, MP
Citation: Mp. Whyte, Hypophosphatasia, GENETICS OF OSTEOPOROSIS AND METABOLIC BONE DISEASE, 2000, pp. 335-356
Authors:
Zucchi, I
Jones, J
Affer, M
Montagna, C
Redolfi, E
Susani, L
Vezzoni, P
Parvari, R
Schlessinger, D
Whyte, MP
Mumm, S
Citation: I. Zucchi et al., Transcription map of Xq27: Candidates for several X-linked diseases, GENOMICS, 57(2), 1999, pp. 209-218
Authors:
Whyte, MP
Eddy, MC
Podgornik, MN
McAlister, WH
Citation: Mp. Whyte et al., Polycystic bone disease: A new, autosomal dominant disorder, J BONE MIN, 14(8), 1999, pp. 1261-1271
Authors:
Fedde, KN
Blair, L
Silverstein, J
Coburn, SP
Ryan, LM
Weinstein, RS
Waymire, K
Narisawa, S
Millan, JL
Macgregor, GR
Whyte, MP
Citation: Kn. Fedde et al., Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasia, J BONE MIN, 14(12), 1999, pp. 2015-2026
Authors:
Reddy, SV
Menaa, C
Singer, FR
Cundy, T
Cornish, J
Whyte, MP
Roodman, GD
Citation: Sv. Reddy et al., Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone, EXP HEMATOL, 27(10), 1999, pp. 1528-1532
Authors:
Moore, CA
Curry, CJR
Henthorn, PS
Smith, JK
Smith, JC
O'Lague, P
Coburn, SP
Weaver, DD
Whyte, MP
Citation: Ca. Moore et al., Mild autosomal dominant hypophosphatasia: In utero presentation in two families, AM J MED G, 86(5), 1999, pp. 410-415
Authors:
Pauli, RM
Modaff, P
Sipes, SL
Whyte, MP
Citation: Rm. Pauli et al., Mild hypophosphatasia mimicking severe osteogenesis imperfecta in utero: Bent but not broken, AM J MED G, 86(5), 1999, pp. 434-438
Authors:
Whyte, MP
Gottesman, GS
Eddy, MC
McAlister, WH
Citation: Mp. Whyte et al., X-linked recessive spondyloepiphyseal dysplasia tarda - Clinical and radiographic evolution in a 6-generation kindred and review of the literature, MEDICINE, 78(1), 1999, pp. 9-25
Authors:
Shaker, JL
Moore, BP
Whyte, MP
Citation: Jl. Shaker et al., Hyperparathyroidism and increased serum IGF-binding protein-2 levels in hepatitis C-associated osteosclerosis, J CLIN END, 84(1), 1999, pp. 384-385
Authors:
Lloyd, SE
Pannett, AAJ
Dixon, PH
Whyte, MP
Thakker, RV
Citation: Se. Lloyd et al., Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13, AM J HU GEN, 64(1), 1999, pp. 189-195
Authors:
Manary, MJ
Hart, CA
Whyte, MP
Citation: Mj. Manary et al., Severe hypophosphatemia in children with kwashiorkor is associated with increased mortality, J PEDIAT, 133(6), 1998, pp. 789-791
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1-24
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