[Hypothalamic syndrome in children with acute leukemia].
Explore the source record for details and available documents.
Acute Disease↗
Biomedical subjects
B V Lebedev
Publications and source records attributed to B V Lebedev.
[Genetic aspects of the clinical diversity of the diseases accompanied by mental retardation].
Explore the source record for details and available documents.
Chromosome Aberrations↗
[Urgent problems of medical genetics in Soviet pediatrics].
Explore the source record for details and available documents.
Anemia, Hemolytic↗
[Intranatal asphyxia and its influence on child development (review of the literature)].
Explore the source record for details and available documents.
Asphyxia Neonatorum↗
[Perspectives on scientific research in the area of child neuropathology].
Explore the source record for details and available documents.
Birth Injuries↗
[State and perspectives of development of neurological and psychiatric service to children in USSR].
Explore the source record for details and available documents.
Child↗
[Clinico-electroencephalographic evaluation of the effectiveness of diet therapy in patients with phenylketonuria].
Explore the source record for details and available documents.
Brain↗
[The guthrie test for the determination of phenylalanine in blood].
Explore the source record for details and available documents.
Child↗
[Mental retardation and hereditary enzymopathy (review)].
Explore the source record for details and available documents.
Ammonia↗
[Medico-genetic problems in pediatrics].
Explore the source record for details and available documents.
Child↗
The "cri du chat" syndrome.
Explore the source record for details and available documents.
Abnormalities, Multiple↗
[Diagnosis of cardiopathy in Friedreich's disease].
Explore the source record for details and available documents.
Child↗
[Diagnosis of the crying cat syndrome].
Explore the source record for details and available documents.
Child, Preschool↗
[Phenylalanine metabolism disorders in phenylketonuria (review)].
Explore the source record for details and available documents.
Humans↗
[Endogenic amino acid imbalance in phenylketonuria].
Explore the source record for details and available documents.
Amino Acids↗
[Determination of heterozygote carrier state of phenylketonuria gene].
Explore the source record for details and available documents.
Adult↗
[Some indices of phenylalanine and tyrosine metabolism in children with phenylketonuria].
Explore the source record for details and available documents.
Adolescent↗
[Experience with treatment of children with phenylketonuria].
Explore the source record for details and available documents.
Child↗