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Birth Defects Original Article Series
|
January 1, 1986
Bone marrow transplantation in type IIa glycogen storage disease
R E Harris, D Hannon, C Vogler, et al.
Die Medizinische Welt
|
February 20, 1981
[Juvenile alpha-1-antitrypsin deficiency. Course, diagnosis and prognosis]
P Abiodun, M Bauer, H Wolf, et al.
American Journal of Diseases of Children (1960)
|
May 1, 1981
Arginine deficiency syndrome. Its occurrence in carbamyl phosphate synthetase deficiency
J J Kline, G Hug, W K Schubert, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine
|
January 1, 1996
Do neuron-specific enolase levels discriminate between small-cell lung cancer and mediastinal tumors?
W Ebert, R Ryll, T Muley, et al.
Journal of the American Chemical Society
|
October 27, 1976
Emission spectroscopy and state ordering of retinals
T Takemura, P K Das, G Hug, et al.
Human Genetics
|
January 1, 1980
Pi Ecincinnati: a new alpha 1-antitrypsin allele in three Negro families
G Hug, G Chuck, T M Slemmer, et al.
Lancet (London, England)
|
September 21, 1974
Letter: Reye's syndrome
T Brown, G Hug, K Bove, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
July 1, 1981
Reye's syndrome simulacra in liver of mice after treatment with chemical agents and encephalomyocarditis virus
G Hug, J Bosken, K Bove, et al.
The Journal of Pediatrics
|
November 1, 1991
Reduction of serum carnitine concentrations during anticonvulsant therapy with phenobarbital, valproic acid, phenytoin, and carbamazepine in children
G Hug, C A McGraw, S R Bates, et al.
American Journal of Diseases of Children (1960)
|
October 1, 1982
Calcitriol deficiency in idiopathic juvenile osteoporosis
H K Marder, R C Tsang, G Hug, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 85) with videos related to
Sort By:
Page
of 9
Birth Defects Original Article Series
|
January 1, 1986
Bone marrow transplantation in type IIa glycogen storage disease
R E Harris, D Hannon, C Vogler, et al.
Die Medizinische Welt
|
February 20, 1981
[Juvenile alpha-1-antitrypsin deficiency. Course, diagnosis and prognosis]
P Abiodun, M Bauer, H Wolf, et al.
American Journal of Diseases of Children (1960)
|
May 1, 1981
Arginine deficiency syndrome. Its occurrence in carbamyl phosphate synthetase deficiency
J J Kline, G Hug, W K Schubert, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine
|
January 1, 1996
Do neuron-specific enolase levels discriminate between small-cell lung cancer and mediastinal tumors?
W Ebert, R Ryll, T Muley, et al.
Journal of the American Chemical Society
|
October 27, 1976
Emission spectroscopy and state ordering of retinals
T Takemura, P K Das, G Hug, et al.
Human Genetics
|
January 1, 1980
Pi Ecincinnati: a new alpha 1-antitrypsin allele in three Negro families
G Hug, G Chuck, T M Slemmer, et al.
Lancet (London, England)
|
September 21, 1974
Letter: Reye's syndrome
T Brown, G Hug, K Bove, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
July 1, 1981
Reye's syndrome simulacra in liver of mice after treatment with chemical agents and encephalomyocarditis virus
G Hug, J Bosken, K Bove, et al.
The Journal of Pediatrics
|
November 1, 1991
Reduction of serum carnitine concentrations during anticonvulsant therapy with phenobarbital, valproic acid, phenytoin, and carbamazepine in children
G Hug, C A McGraw, S R Bates, et al.
American Journal of Diseases of Children (1960)
|
October 1, 1982
Calcitriol deficiency in idiopathic juvenile osteoporosis
H K Marder, R C Tsang, G Hug, et al.
Page
of 9