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Search Results - Scholem, R
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The Clinical and Biochemical Spectrum of Human Pyruvate Dehydrogenase Complex Deficiency
by
BROWN, G. K.
,
BROWN, R. M.
,
SCHOLEM, R. D.
,
KIRBY, D. M.
,
DAHL, H-H. M.
Published in
Annals of the New York Academy of Sciences
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Immunochemical analysis of normal and mutant forms of human pyruvate dehydrogenase
by
Wicking, C A
,
Scholem, R D
,
Hunt, S M
,
Brown, G K
Published in
Biochemical journal
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"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis
by
Brown, G K
,
Haan, E A
,
Kirby, D M
,
Scholem, R D
,
Wraith, J E
,
Rogers, J G
,
Danks, D M
Published in
European journal of pediatrics
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Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defect
by
HAAN, E. A
,
SCHOLEM, R. D
,
CROLL, H. B
,
BROWN, G. K
Published in
European journal of pediatrics
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Metabolism of malonic semialdehyde in man
by
Scholem, R D
,
Brown, G K
Published in
Biochemical journal
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beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformations
by
Brown, G K
,
Hunt, S M
,
Scholem, R
,
Fowler, K
,
Grimes, A
,
Mercer, J F
,
Truscott, R M
,
Cotton, R G
,
Rogers, J G
,
Danks, D M
Published in
Pediatrics (Evanston)
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Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria
by
HAAN, E. A
,
SCHOLEM, R. D
,
PITT, J. J
,
WRAITH, J. E
,
BROWN, G. K
Published in
European journal of pediatrics
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Cerebral lactic acidosis: defects in pyruvate metabolism with profound braindamage and minimal systemic acidosis
by
BROWN, G. K
,
HAAN, E. A
,
KIRBY, D. M
,
SCHOLEM, R. D
,
WRAITH, J. E
,
ROGERS, J. G
,
DANKS, D. M
Published in
European journal of pediatrics
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Origins of the Kabbalah
by
Schafer, Peter
,
Scholem, Gershom
,
Werblowsky, R. J. Zwi
,
Arkush, Allan
Published in
Numen
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Kabbalah
by
Greenfield, Jonas C.
,
Scholem, Gershom
,
Scholem, Gershom G.
,
Werblowsky, R. J. Zwi
Published in
Journal of the American Oriental Society
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