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Results of search for 'au:"Whyte, M"', page 8 of 14
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Authors
Avioli, L V
Bergfeld, M A
Chines, A
Coburn, S P
Eddy, M C
Fallon, M D
Fedde, K N
Henthorn, P S
Hughes, J M
McAlister, W H
Mumm, S
Murphy, W A
Sabroe, I
Teitelbaum, S L
Thakker, R V
Whyte, M
Whyte, M K
Whyte, M K B
Whyte, M P
Wooding, C
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Adolescent
Adult
Alkaline Phosphatase
Child
Child, Preschool
Female
Humans
Hypophosphatasia
Infant
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Pedigree
Radiography
blood
complications
diagnostic imaging
enzymology
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141.
Normal left ventricular performance documented by Doppler echocardiography in patients with long-standing hypocalcemia.
[electronic resource]
by
Vered, I
Vered, Z
Perez, J E
Jaffe, A S
Whyte, M P
Producer:
19890502
In:
The American journal of medicine
vol. 86
Online resources:
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142.
Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin.
[electronic resource]
by
Mumm, S
Zhang, X
Gottesman, G S
McAlister, W H
Whyte, M P
Producer:
20020603
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
vol. 16
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143.
mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation.
[electronic resource]
by
Mumm, S
Whyte, M P
Thakker, R V
Buetow, K H
Schlessinger, D
Producer:
19970123
In:
American journal of human genetics
vol. 60
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144.
Audiologic findings in young patients with hypophosphatemic bone disease.
[electronic resource]
by
Meister, M
Johnson, A
Popelka, G R
Kim, G S
Whyte, M P
Producer:
19860925
In:
The Annals of otology, rhinology, and laryngology
vol. 95
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145.
Differing lumbar vertebral mineralization rates in ambulatory pediatric patients with osteogenesis imperfecta.
[electronic resource]
by
Reinus, W R
McAlister, W H
Schranck, F
Chines, A
Whyte, M P
Producer:
19980312
In:
Calcified tissue international
vol. 62
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146.
Normal left ventricular performance in children with X-linked hypophosphatemic rickets: a Doppler echocardiography study.
[electronic resource]
by
Vered, I
Vered, Z
Perez, J E
Jaffe, A S
Whyte, M P
Producer:
19900813
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
vol. 5
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147.
Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders.
[electronic resource]
by
Whyte, M P
Chines, A
Silva, D P
Landt, Y
Ladenson, J H
Producer:
19970130
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
vol. 11
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148.
Extraskeletal osteoclastomas responsive to dexamethasone treatment in Paget bone disease.
[electronic resource]
by
Ziambaras, K
Totty, W A
Teitelbaum, S L
Dierkes, M
Whyte, M P
Producer:
19971125
In:
The Journal of clinical endocrinology and metabolism
vol. 82
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149.
CT-guided extrapleural drainage of bronchogenic cyst.
[electronic resource]
by
Adam, A
MacSweeney, J E
Whyte, M K
Smith, P L
Ind, P W
Producer:
19891226
In:
Journal of computer assisted tomography
vol. 13
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150.
Bilateral granulomatous uveitis in association with common variable immunodeficiency.
[electronic resource]
by
Cohen, V M
Lee, J A
Egner, W
Whyte, M K
Rennie, I G
Producer:
20010521
In:
The British journal of ophthalmology
vol. 85
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151.
The rise and rise of Staphylococcus aureus: laughing in the face of granulocytes.
[electronic resource]
by
Anwar, S
Prince, L R
Foster, S J
Whyte, M K B
Sabroe, I
Producer:
20090910
In:
Clinical and experimental immunology
vol. 157
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152.
Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies.
[electronic resource]
by
Thakker, R V
Davies, K E
Whyte, M P
Wooding, C
O'Riordan, J L
Producer:
19900813
In:
The Journal of clinical investigation
vol. 86
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153.
X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene.
[electronic resource]
by
Christie, P T
Harding, B
Nesbit, M A
Whyte, M P
Thakker, R V
Producer:
20010906
In:
The Journal of clinical endocrinology and metabolism
vol. 86
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154.
Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasia.
[electronic resource]
by
Henthorn, P S
Raducha, M
Fedde, K N
Lafferty, M A
Whyte, M P
Producer:
19921117
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 89
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155.
Transient elevations of cytosolic free calcium retard subsequent apoptosis in neutrophils in vitro.
[electronic resource]
by
Whyte, M K
Hardwick, S J
Meagher, L C
Savill, J S
Haslett, C
Producer:
19930812
In:
The Journal of clinical investigation
vol. 92
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156.
Management and prevention of vitamin D deficiency rickets in captive-born juvenile chimpanzees (Pan troglodytes).
[electronic resource]
by
Junge, R E
Gannon, F H
Porton, I
McAlister, W H
Whyte, M P
Producer:
20010920
In:
Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians
vol. 31
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157.
Idiopathic multicentric osteolysis. Report of an affected father and son.
[electronic resource]
by
Whyte, M P
Murphy, W A
Kleerekoper, M
Teitelbaum, S L
Avioli, L V
Producer:
19780617
In:
Arthritis and rheumatism
vol. 21
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158.
Systemic mastocytosis.
[electronic resource]
by
Korenblat, P E
Wedner, H J
Whyte, M P
Frankel, S
Avioli, L V
Producer:
19841130
In:
Archives of internal medicine
vol. 144
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159.
Effect of percutaneous transcatheter embolization on pulmonary function, right-to-left shunt, and arterial oxygenation in patients with pulmonary arteriovenous malformations.
[electronic resource]
by
Chilvers, E R
Whyte, M K
Jackson, J E
Allison, D J
Hughes, J M
Producer:
19900911
In:
The American review of respiratory disease
vol. 142
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160.
Adult hypophosphatasia. Clinical, laboratory, and genetic investigation of a large kindred with review of the literature.
[electronic resource]
by
Whyte, M P
Teitelbaum, S L
Murphy, W A
Bergfeld, M A
Avioli, L V
Producer:
19791121
In:
Medicine
vol. 58
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