[Pentosuria in a non-thriving child].
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Carbohydrate Metabolism, Inborn Errors↗
Biomedical subjects
B Blehová
Publications and source records attributed to B Blehová.
[Melanogenesis in hair of phenylketonurics (author's transl)].
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Child, Preschool↗
[Hyperphenylalaninemia due to digydropteridine-reductase deficiency].
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Child, Preschool↗
[A mother with hyperphenylalaninemia and development of the fetus during a diet in pregnancy].
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Female↗
Trisomy 9p resulting from maternal 9/21 translocation.
The clinical picture found in a child with trisomy 9p confirmed that this chromosomal syndrome is a entity, which arises from maternal translocation t(9;21).
Abnormalities, Multiple↗
[Evaluation of screening for phenylketonuria after 6 years of existence of the laboratory].
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Czechoslovakia↗
[Effect of D-penicillamine in scleroderma complicating phenylketonuria].
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Child, Preschool↗
[Mother with phenylketonuria and foetal development].
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Female↗
[Alkaptonuria in a newborn infant].
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Alkaptonuria↗
[Triplets, 2 of which are twins with phenylketonuria].
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Adult↗
Robertsonian translocation between the chromosome Y and 15.
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Adult↗
[Development of children diagnosed at the maternity hospital using Guthrie's method in comparison with children diagnosed later and children untreated].
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Child, Preschool↗
[Hyperprolinuria].
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Amino Acid Metabolism, Inborn Errors↗
Iminoglycinuria in a child in Czechoslovakia.
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Amino Acid Metabolism, Inborn Errors↗
New approach to the treatment of mucopolysaccharidoses by plasma and leucocyte transfusions.
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Adolescent↗
[Syndrome 4p-].
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Abnormalities, Multiple↗
[Problems with diet in phenylketonuria].
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Diet Therapy↗