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51

Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders

Michael P. Whyte, Arkadi Chines, David P. Silva Jr., Yvonne Landt, Jack H. Ladenson

Journal:

Journal of Bone and Mineral Research

Year:

1996

Language:

english

File:

PDF, 637 KB

english, 1996

52

Evidence against a role for alkaline phosphatase in the dephosphorylation of plasma membrane proteins: Hypophosphatasia fibroblast study

Kenton N. Fedde, Michelle P. Michel, Michael P. Whyte

Journal:

Journal of Cellular Biochemistry

Year:

1993

Language:

english

File:

PDF, 753 KB

english, 1993

53

Features of the Caribbean low level jet

Felicia S. Whyte, Michael A. Taylor, Tannecia S. Stephenson, Jayaka D. Campbell

Journal:

International Journal of Climatology

Year:

2008

Language:

english

File:

PDF, 1021 KB

english, 2008

54

Infantile hypophosphatasia: Successful prenatal assessment by testing for tissue-non-specific alkaline phosphatase isoenzyme gene mutations

Paula S. Henthorn, Dr Michael P. Whyte

Journal:

Prenatal Diagnosis

Year:

1995

Language:

english

File:

PDF, 660 KB

english, 1995

55

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH

Dorothy Trump, Michael P. Whyte, Carol Wooding, Joanna T. Pang, Simon H. S. Pearce, David B. Kocher, Rajesh V. Thakker

Journal:

Year:

1995

Language:

english

File:

PDF, 541 KB

english, 1995

56

Mixed-sclerosing-bone-dystrophy: Report of a case and review of the literature

Michael P. Whyte, William A. Murphy, Michael D. Fallon, Theodore J. Hahn

Journal:

Skeletal Radiology

Year:

1981

Language:

english

File:

PDF, 2.59 MB

english, 1981

57

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

William H. McAlister, Jeffrey D. Coe, Michael P. Whyte

Journal:

Skeletal Radiology

Year:

1986

Language:

english

File:

PDF, 1.94 MB

english, 1986

58

Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemia

Cynthia T. McMurtry, Francine W. Schranck, Denise A. Walkenhorst, William A. Murphy, David B. Kocher, Steven L. Teitelbaum, Reta C. Rupich, Michael P. Whyte

Journal:

Pediatric Nephrology

Year:

1993

Language:

english

File:

PDF, 112 KB

english, 1993

59

Infantile hypophosphatasia: Enzymatic defect explored with alkaline phosphatase-deficient skin fibroblasts in culture

Michael P. Whyte, Steven D. Rettinger, Lauri A. Vrabel

Journal:

Calcified Tissue International

Year:

1987

Language:

english

File:

PDF, 912 KB

english, 1987

60

Infantile hypophosphatasia fibroblasts proliferate normally in culture: Evidence against a role for alkaline phosphatase (tissue nonspecific isoenzyme) in the regulation of cell growth and differentiation

Michael P. Whyte, Lauri A. Vrabel

Journal:

Calcified Tissue International

Year:

1987

Language:

english

File:

PDF, 687 KB

english, 1987

61

Mixed-sclerosing-bone-dystrophy: 42-year follow-up of a case reported as osteopetrosis

Roberto Pacifici, William A. Murphy, Steven L. Teitelbaum, Michael P. Whyte

Journal:

Calcified Tissue International

Year:

1986

Language:

english

File:

PDF, 5.76 MB

english, 1986

62

Feedback

William F. Whyte, William H. Friedland, Harry Edwards, William D. Cabin, Michael Lipsky, David J. Olson

Journal:

Year:

1969

Language:

english

File:

PDF, 97 KB

english, 1969

63

Review of interventional procedures in the very low birth-weight infant (

Eoghan E. Laffan, Patrick J. McNamara, Joao Amaral, Hilary Whyte, Johanne L’Herault, Michael Temple, Philip John, Bairbre L. Connolly

Journal:

Pediatric Radiology

Year:

2009

Language:

english

File:

PDF, 170 KB

english, 2009

64

Clinical and biochemical correlates of insoluble α-synuclein in dementia with Lewy bodies

Jochen Klucken, Martin Ingelsson, Youngah Shin, Michael C. Irizarry, E. T. Hedley-Whyte, Matthew P. Frosch, John H. Growdon, Pamela J. McLean, Bradley T. Hyman

Journal:

Acta Neuropathologica

Year:

2006

Language:

english

File:

PDF, 533 KB

english, 2006

65

Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome

Giles D.J. Watts, Sarju G. Mehta, Chengfeng Zhao, Sheena Ramdeen, Sara Jane Hamilton, Deborah V. Novack, Steven Mumm, Michael P. Whyte, Barbara Mc Gillivray, Virginia E. Kimonis

Journal:

Year:

2005

Language:

english

File:

PDF, 317 KB

english, 2005

66

Dose-escalation with proton/photon irradiation for Daumas-Duport lower-grade glioma: results of an institutional phase I/II trial

Markus M Fitzek, Allan F Thornton, Griffith Harsh IV, James D Rabinov, John E Munzenrider, Michael Lev, Marek Ancukiewicz, Marc Bussiere, E.Tessa Hedley-Whyte, Fred H Hochberg, Francisco S Pardo

Journal:

International Journal of Radiation Oncology*Biology*Physics

Year:

2001

Language:

english

File:

PDF, 141 KB

english, 2001

67

Biochemical and Ultrastructural Demonstration of Elastin Accumulation in the Skin Lesions of the Buschke-Ollendorff Syndrome.

Uitto, Jouni, Cruz, Daniel J. Santa, Starcher, Barry C., Whyte, Michael P., Murphy, William A.

Journal:

The Journal of Investigative Dermatology

Year:

1981

File:

PDF, 2.15 MB

1981

68

Questioning context: a set of interdisciplinary questions for investigating contextual factors affecting health decision making

Andrea Charise, Holly Witteman, Sarah Whyte, Erica J. Sutton, Jacqueline L. Bender, Michael Massimi, Lindsay Stephens, Joshua Evans, Carmen Logie, Raza M. Mirza, Marie Elf

Journal:

Health Expectations

Year:

2011

Language:

english

File:

PDF, 194 KB

english, 2011

69

The phenol red thread test for lacrimal volume – does it matter if the eyes are open or closed?

Michael J. Doughty, Julie Whyte, Wendy Li

Journal:

Ophthalmic and Physiological Optics

Year:

2007

Language:

english

File:

PDF, 535 KB

english, 2007

70

Onset of Depression in Elderly Persons After Hip Fracture: Implications for Prevention and Early Intervention of Late-Life Depression

Eric J. Lenze, Michael C. Munin, Elizabeth R. Skidmore, Mary Amanda Dew, Joan C. Rogers, Ellen M. Whyte, Tanya Quear, Amy Begley, Charles F. Reynolds III

Journal:

Journal of the American Geriatrics Society

Year:

2007

Language:

english

File:

PDF, 89 KB

english, 2007

71

Chloroquine effects in Dictyostelium discoideum: Inhibition of other enzymes besides the cathepsin B

Michael J. North, Anne Whyte, Andrew Ventom

Journal:

FEMS Microbiology Letters

Year:

1982

Language:

english

File:

PDF, 241 KB

english, 1982

72

Chemiluminescence of peripheral polymorphonuclear leukocytes from adult periodontitis patients

G. J. Whyte, Gregory J. Seymour, Kee Cheung, Michael F. Robinson

Journal:

Journal of Clinical Periodontology

Year:

1989

Language:

english

File:

PDF, 2.52 MB

english, 1989

73

Amphetamine-induced movement disorder

Michael A Downes, Ian M Whyte

Journal:

Emergency Medicine Australasia

Year:

2005

Language:

english

File:

PDF, 68 KB

english, 2005

74

Physiological role of alkaline phosphatase explored in hypophosphatasia

Michael P. Whyte

Journal:

Annals of the New York Academy of Sciences

Year:

2010

Language:

english

File:

PDF, 290 KB

english, 2010

75

10.1038/71667

Hughes, Anne E., Ralston, Stuart H., Marken, John, Bell, Christine, MacPherson, Heather, Wallace, Richard G.H., van Hul, Wim, Whyte, Michael P., Nakatsuka, Kyoshi, Hovy, Louis, Anderson, Dirk M.

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 385 KB

english, 2000

76

Interleukin 18 receptor 1 gene polymorphisms are associated with asthma

Zhu, Guohua, Whyte, Moira K B, Vestbo, Jorgen, Carlsen, Karin, Carlsen, Kai-Håkon, Lenney, Warren, Silverman, Michael, Helms, Peter, Pillai, Sreekumar G

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 173 KB

english, 2008

77

Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3

Hannan, Fadil M, Nesbit, M Andrew, Turner, Jeremy J O, Stacey, Joanna M, Cianferotti, Luisella, Christie, Paul T, Conigrave, Arthur D, Whyte, Michael P, Thakker, Rajesh V

Journal:

European Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 427 KB

english, 2009

78

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

Watts, Giles D J, Wymer, Jill, Kovach, Margaret J, Mehta, Sarju G, Mumm, Steven, Darvish, Daniel, Pestronk, Alan, Whyte, Michael P, Kimonis, Virginia E

Journal:

Nature Genetics

Year:

2004

Language:

english

File:

PDF, 708 KB

english, 2004

79

ANGIOKERATOMA SERPIGINOSUM

MICHAEL P. WHYTE

Journal:

International Journal of Dermatology

Year:

1978

Language:

english

File:

PDF, 1.61 MB

english, 1978

80

Paget's Disease of Bone and Genetic Disorders of RANKL/OPG/RANK/NF-κB Signaling

MICHAEL P. WHYTE

Journal:

Annals of the New York Academy of Sciences

Year:

2006

Language:

english

File:

PDF, 154 KB

english, 2006

81

Oropharyngeal Skeletal Disease Accompanying High Bone Mass and Novel LRP5 Mutation

Michael R Rickels, Xiafang Zhang, Steven Mumm, Michael P Whyte

Journal:

Journal of Bone and Mineral Research

Year:

2005

Language:

english

File:

PDF, 712 KB

english, 2005

82

Recovery From Skeletal Fluorosis (an Enigmatic, American Case)

Etah S Kurland, Rifka C Schulman, Joseph E Zerwekh, William R Reinus, David W Dempster, Michael P Whyte

Journal:

Journal of Bone and Mineral Research

Year:

2007

Language:

english

File:

PDF, 4.65 MB

english, 2007

83

Deactivating Germline Mutations in LEMD3 Cause Osteopoikilosis and Buschke-Ollendorff Syndrome, but Not Sporadic Melorheostosis

Steven Mumm, Deborah Wenkert, Xiafang Zhang, William H McAlister, Richard J Mier, Michael P Whyte

Journal:

Journal of Bone and Mineral Research

Year:

2007

Language:

english

File:

PDF, 3.11 MB

english, 2007

84

Juvenile Paget's Disease: The Second Reported, Oldest Patient Is Homozygous for the TNFRSF11B “Balkan” Mutation (966_969delTGACinsCTT), Which Elevates Circulating Immunoreactive Osteoprotegerin Levels

Michael P Whyte, Panagiotis N Singhellakis, Michael B Petersen, Michael Davies, William G Totty, Steven Mumm

Journal:

Journal of Bone and Mineral Research

Year:

2007

Language:

english

File:

PDF, 2.41 MB

english, 2007

85

Recovery From Skeletal Fluorosis

Etah S Kurland, Michael P Whyte

Journal:

Journal of Bone and Mineral Research

Year:

2007

Language:

english

File:

PDF, 35 KB

english, 2007

86

Skeletal Fluorosis From Instant Tea

Michael P Whyte, William G Totty, Vivienne T Lim, Gary M Whitford

Journal:

Journal of Bone and Mineral Research

Year:

2008

Language:

english

File:

PDF, 423 KB

english, 2008

87

Bisphosphonate-Induced Osteopetrosis: Novel Bone Modeling Defects, Metaphyseal Osteopenia, and Osteosclerosis Fractures After Drug Exposure Ceases

Michael P Whyte, William H McAlister, Deborah V Novack, Karen L Clements, Perry L Schoenecker, Deborah Wenkert

Journal:

Journal of Bone and Mineral Research

Year:

2008

Language:

english

File:

PDF, 1.12 MB

english, 2008

88

Atypical Femoral Fractures, Bisphosphonates, and Adult Hypophosphatasia

Michael P Whyte

Journal:

Journal of Bone and Mineral Research

Year:

2009

Language:

english

File:

PDF, 614 KB

english, 2009

89

Chronic Recurrent Multifocal Osteomyelitis Mimicked in Childhood Hypophosphatasia

Michael P Whyte, Deborah Wenkert, William H McAlister, M Zulf Mughal, Anthony J Freemont, Richard Whitehouse, Eileen M Baildam, Stephen P Coburn, Lawrence M Ryan, Steven Mumm

Journal:

Journal of Bone and Mineral Research

Year:

2009

Language:

english

File:

PDF, 2.05 MB

english, 2009

90

Linkage Studies of a Missouri Kindred with Autosomal Dominant Spondyloepimetaphyseal Dysplasia (SEMD) Indicate Genetic Heterogeneity

Joseph M. Gertner, Michael P. Whyte, Peter H. Dixon, Joanna T. Pang, Dorothy Trump, Simon H. S. Pearce, Carol Wooding, Rajesh V. Thakker

Journal:

Journal of Bone and Mineral Research

Year:

1997

Language:

english

File:

PDF, 282 KB

english, 1997

91

Alkaline Phosphatase Knock-Out Mice Recapitulate the Metabolic and Skeletal Defects of Infantile Hypophosphatasia

Kenton N. Fedde, Libby Blair, Julie Silverstein, Stephen P. Coburn, Lawrence M. Ryan, Robert S. Weinstein, Katrina Waymire, Sonoko Narisawa, José L. Millán, Grant R. Macgregor, Michael P. Whyte

Journal:

Journal of Bone and Mineral Research

Year:

1999

Language:

english

File:

PDF, 6.10 MB

english, 1999

92

Polycystic Bone Disease: A New, Autosomal Dominant Disorder

Dr. Michael P. Whyte, Mark C. Eddy, Michelle N. Podgornik, William H. Mcalister

Journal:

Journal of Bone and Mineral Research

Year:

1999

Language:

english

File:

PDF, 385 KB

english, 1999

93

Deficiency of the α-Subunit of the Stimulatory G Protein and Severe Extraskeletal Ossification

Mark C. Eddy, Suzanne M. Jan de beur, Suzanne M. Yandow, William H. McAlister, Eileen M. Shore, Frederick S. Kaplan, Michael P. Whyte, Michael A. Levine

Journal:

Journal of Bone and Mineral Research

Year:

2000

Language:

english

File:

PDF, 1.95 MB

english, 2000

94

Expansile Skeletal Hyperphosphatasia: A New Familial Metabolic Bone Disease

Michael P. Whyte, Barbara G. Mills, William R. Reinus, Michelle N. Podgornik, G. David Roodman, Francis H. Gannon, Mark C. Eddy, William H. Mcalister

Journal:

Journal of Bone and Mineral Research

Year:

2000

Language:

english

File:

PDF, 3.86 MB

english, 2000

95

Polycystic Bone Disease

Michael P. Whyte, Mark C. Eddy, Michelle N. Podgornik, William H. McAlister

Journal:

Journal of Bone and Mineral Research

Year:

2000

Language:

english

File:

PDF, 98 KB

english, 2000

96

Preonset Studies of Spondyloepiphyseal Dysplasia Tarda Caused by a Novel 2-Base Pair Deletion in SEDL Encoding Sedlin

Steven Mumm, Xiafang Zhang, Gary S. Gottesman, William H. McAlister, Michael P. Whyte

Journal:

Journal of Bone and Mineral Research

Year:

2001

Language:

english

File:

PDF, 973 KB

english, 2001

97

Pseudo-(Tumor-Induced) Rickets

Michael P. Whyte, Michelle N. Podgornik, Valerie A. Wollberg, Mark C. Eddy, William H. McAlister

Journal:

Journal of Bone and Mineral Research

Year:

2001

Language:

english

File:

PDF, 588 KB

english, 2001

98

Historical Vignette: Hypophosphatasia: Molecular Diagnosis of Rathbun's Original Case

Steven Mumm, Jonathan Jones, Patrick Finnegan, Michael P. Whyte

Journal:

Journal of Bone and Mineral Research

Year:

2001

Language:

english

File:

PDF, 549 KB

english, 2001

99

Expansile Skeletal Hyperphosphatasia Is Caused by a 15-Base Pair Tandem Duplication in TNFRSF11A Encoding RANK and Is Allelic to Familial Expansile Osteolysis

Michael P. Whyte, Anne E. Hughes

Journal:

Journal of Bone and Mineral Research

Year:

2002

Language:

english

File:

PDF, 197 KB

english, 2002

100

Marrow Cell Transplantation for Infantile Hypophosphatasia

Michael P Whyte, Joanne Kurtzberg, William H McALISTER, Steven Mumm, Michelle N Podgornik, Stephen P Coburn, Lawrence M Ryan, Cindy R Miller, Gary S Gottesman, Alan K Smith, Judy Douville, Barbara Wat

Journal:

Journal of Bone and Mineral Research

Year:

2003

Language:

english

File:

PDF, 1.42 MB

english, 2003