[EEG studies in totally and almost blind children].
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Adolescent↗
Biomedical subjects
H Kaloud
Publications and source records attributed to H Kaloud.
[Activity of galactose-1-phosphate uridyl transferase in erythrocytes of healthy children and adults (contribution to the diagnosis of galactosemia)].
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Adult↗
[Clinical and biochemical findings in a child with hereditary galactokinase defect].
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Clinical Enzyme Tests↗
[Hydrated ergot alkaloids in cases of respiratory-distress-syndrome (RDS). 1].
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Animals↗
[Gene frequency of hereditary galactosemia with reference to the Duarte variant].
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Adolescent↗
[Make the diagnosis].
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Central Nervous System Diseases↗
[Experiences with a new chemotherapeutic agent in urinary tract infections in infants].
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Journal Article↗
[Activity of galaktose-1-phosphate-uridyltransferase in erythrozytes of galactosemia heterocygotes of different ages (author's transl)].
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Adult↗
[XX-XXX chromosomal mosaicism in an newborn with multiple malformations (author's transl)].
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Abnormalities, Multiple↗
[Somatic development and motor activity of blind children].
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Anthropometry↗
[Galactose-1-phosphate-uridyltransferase in erythrocytes of children with hepatitis epidemica].
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Adolescent↗
EEG investigations in children with lesions in the peripheral part of the visual system.
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Blindness↗
[Acute form of galactosemia in siblings].
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Acute Disease↗
[Mother and child from the viewpoint of modern pediatrics].
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Child Abuse↗
[Mother and child from the viewpoint of modern pediatrics].
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Child Health Services↗
[The importance of fetofetal transfusion].
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Abruptio Placentae↗
[A new device for exchange transfusions].
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Blood Group Incompatibility↗
[Catamnestic studies of measles encephalitis].
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Adolescent↗