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Medicine
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January 1, 1984
Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult forms
M D Fallon, S L Teitelbaum, R S Weinstein, et al.
Journal of Inherited Metabolic Disease
|
February 22, 2000
Increased urine heparan and chondroitin sulphate excretion in patients with osteopetrosis
R D Steiner, M P Whyte, E Chang, et al.
Pediatric Radiology
|
May 1, 1997
Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864
T E Herman, A Chines, W H McAlister, et al.
Connective Tissue Research
|
January 1, 1989
First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralization
M J Weiss, D E Cole, K Ray, et al.
Experimental Hematology
|
October 12, 1999
Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone
S V Reddy, C Menaa, F R Singer, et al.
The Journal of Clinical Investigation
|
April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphatase
M P Whyte, J D Mahuren, K N Fedde, et al.
Medicine
|
November 1, 1989
X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adults
I R Reid, D C Hardy, W A Murphy, et al.
The New England Journal of Medicine
|
April 10, 1986
Increased serum pyridoxal-5'-phosphate in pseudohypophosphatasia
D E Cole, S R Salisbury, R A Stinson, et al.
The American Journal of Medicine
|
January 1, 1991
X-linked hypophosphatemia: skeletal mass in adults assessed by histomorphometry, computed tomography, and absorptiometry
I R Reid, W A Murphy, D C Hardy, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1988
A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia
M J Weiss, D E Cole, K Ray, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 166) with videos related to
Sort By:
Page
of 17
Medicine
|
January 1, 1984
Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult forms
M D Fallon, S L Teitelbaum, R S Weinstein, et al.
Journal of Inherited Metabolic Disease
|
February 22, 2000
Increased urine heparan and chondroitin sulphate excretion in patients with osteopetrosis
R D Steiner, M P Whyte, E Chang, et al.
Pediatric Radiology
|
May 1, 1997
Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864
T E Herman, A Chines, W H McAlister, et al.
Connective Tissue Research
|
January 1, 1989
First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralization
M J Weiss, D E Cole, K Ray, et al.
Experimental Hematology
|
October 12, 1999
Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone
S V Reddy, C Menaa, F R Singer, et al.
The Journal of Clinical Investigation
|
April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphatase
M P Whyte, J D Mahuren, K N Fedde, et al.
Medicine
|
November 1, 1989
X-linked hypophosphatemia: a clinical, biochemical, and histopathologic assessment of morbidity in adults
I R Reid, D C Hardy, W A Murphy, et al.
The New England Journal of Medicine
|
April 10, 1986
Increased serum pyridoxal-5'-phosphate in pseudohypophosphatasia
D E Cole, S R Salisbury, R A Stinson, et al.
The American Journal of Medicine
|
January 1, 1991
X-linked hypophosphatemia: skeletal mass in adults assessed by histomorphometry, computed tomography, and absorptiometry
I R Reid, W A Murphy, D C Hardy, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1988
A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia
M J Weiss, D E Cole, K Ray, et al.
Page
of 17