[Ornithinemia, a newly recognized amino acid metabolism disorder with brain damage].
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Amino Acid Metabolism, Inborn Errors↗
Biomedical subjects
H Bickel
Publications and source records attributed to H Bickel.
[Methods of thin-layer chromatography for the identification of aminoaciduria, aminoacidemia and galactosemia].
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Adult↗
Ornithinaemia. Another disorder of aminoacid metabolism associated with brain damage.
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Amino Acid Metabolism, Inborn Errors↗
[Ornithinemia, additional disorder of amino acid metabolism with brain damage].
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Amino Acids↗
[Concerning the preparation of 7-amino-cephalosporanic acid].
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Cephalosporins↗
[Changed activities of metabolic enyymes in thrombocytes of patients with liver cirrhosis and splenomegaly].
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Blood Platelets↗
[Data on levorin A and candicidin].
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Actinomyces↗
[Brain electric studies].
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Central Nervous System Diseases↗
[On phenylketonuria. Carrying out of phenylalanine-low diet].
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Child↗
[Brain atrophy and disorders of the amino acid metabolism].
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Amino Acid Metabolism, Inborn Errors↗
[Metabolism and metabolic diseases].
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Adult↗
[Wilson's disease (hepatolenticular degeneration)].
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Adolescent↗
[Early diagnosis of phenylketonuria].
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Humans↗
New derivatives of rifamycin antibiotics.
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Chemical Phenomena↗
[Hereditary forms of tubular kidney disease: advances in diagnosis and therapy].
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Acidosis, Renal Tubular↗
[Early diagnosis of mental deficiency caused by metabolic diseases in children].
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Galactosemias↗
Constitution of ferrimycin A1.
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Anti-Bacterial Agents↗
[Recent findings on hepatocerebral degeneration (Wilson's disease)].
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Hepatolenticular Degeneration↗