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1.
Partial deletion of the long arm chromosome 11 in Jacobsen syndrome.
Reddy, K S; Thomas, I M; Narayanan, H S.
Indian J Pediatr ; 1986 Jan-Feb; 53(1): 123-6
Article in English | IMSEAR | ID: sea-79022

Subject(s)
Chromosome Deletion , Chromosomes, Human, Pair 11 , Humans , Infant , Male , Syndrome
2.
Partial deletion of the long arm of chromosome 11 the Jacobsen syndrome.
Reddy, K S; Thomas, I M; Narayanan, H S.
Indian J Pediatr ; 1984 May-Jun; 51(410): 359-62
Article in English | IMSEAR | ID: sea-79730

Subject(s)
Abnormalities, Multiple/genetics , Chromosome Deletion , Chromosomes, Human, 6-12 and X , Humans , Infant , Karyotyping , Male , Syndrome
3.
Monitoring of serum lithium levels in manic depressive psychosis.
Subhash, M N; Narayanan, H S; Rao, B S; Channabasavanna, S M.
Article in English | IMSEAR | ID: sea-19381

Subject(s)
Adult , Bipolar Disorder/blood , Female , Follow-Up Studies , Humans , Lithium/blood , Male
4.
Laurence-Moon-Biedl-Bardet syndrome; review of 14 cases.
Narayanan, H S; Rao, B S; Reddy, G N.
Indian J Med Sci ; 1977 Feb; 31(2): 30-2
Article in English | IMSEAR | ID: sea-67917

Subject(s)
Adolescent , Adult , Child , Child, Preschool , Consanguinity , Female , Humans , Infant , Laurence-Moon Syndrome/genetics , Male , Pedigree
5.
Metabolic anomalies detected during a systematic biochemical screening of mentally retarded cases.
Rao, B S; Subhash, M N; Narayanan, H S.
Article in English | IMSEAR | ID: sea-26120

Subject(s)
Adolescent , Amino Acid Metabolism, Inborn Errors/epidemiology , Child , Child, Preschool , Female , Humans , India , Infant , Male , Intellectual Disability/etiology , Phenylketonurias/epidemiology
6.
Hydroxyprolinemia: a case report.
Rama Rao, B S; Subhash, M N; Narayanan, H S.
Indian Pediatr ; 1974 Dec; 11(12): 829-30
Article in English | IMSEAR | ID: sea-6863

Subject(s)
Amino Acid Metabolism, Inborn Errors , Child , Humans , Hydroxyproline/blood , Male
7.
Histidinemia. Report of a case.
Rao, S R; Subhash, M N; Narayanan, H S.
Indian J Pediatr ; 1974 Sep; 41(320): 312-3
Article in English | IMSEAR | ID: sea-82536

Subject(s)
Amino Acid Metabolism, Inborn Errors , Child , Histidine/blood , Humans , Male
8.
A comparative double-blind evaluation of iprindole and imipramine in the treatment of depressive states.
Narayanan, H S; Reddy, G N; Rao, B S.
Indian J Med Sci ; 1973 Jan; 27(1): 1-7
Article in English | IMSEAR | ID: sea-67987

Subject(s)
Adult , Antidepressive Agents/therapeutic use , Clinical Trials as Topic , Depression/drug therapy , Female , Humans , Imipramine/adverse effects , Indoles/therapeutic use , Iprindole/adverse effects , Male , Middle Aged
9.
Homocystinuria in three Indian children.
Rao, R; Sridhara, B S; Narayanan, H S; Reddy, G N.
Article in English | IMSEAR | ID: sea-26145

Subject(s)
Abnormalities, Multiple/diagnosis , Child , Child, Preschool , Diagnosis, Differential , Female , Homocystinuria/diagnosis , Humans , Male , Intellectual Disability/diagnosis , Methionine/metabolism
10.
Neurological, psychiatric and genetic investigations of phenylketonuria.
Narayanan, H S; Reddy, G N; Salgunan, N; Rama Rao, B S.
Neurol India ; 1971 Mar; 19(1): 38-42
Article in English | IMSEAR | ID: sea-121320

Subject(s)
Child , Child, Preschool , Humans , Neurologic Examination , Pedigree , Phenylketonurias/genetics , Psychological Tests
11.
Investigations on urinary excretion of 3,4 dimethoxyphenylethylamine (the pink spot), the Mauve factor and aromatic compounds in patients with schizophrenia.
Rao, B S; Narayanan, H S; Reddy, G N.
Article in English | IMSEAR | ID: sea-22215

Subject(s)
Humans , Phenethylamines/urine , Schizophrenia/urine
12.
Homocystinuria.
Rao, B S; Narayanan, H S; Reddy, G N.
Indian J Pediatr ; 1971 Jan; 38(276): 37-8
Article in English | IMSEAR | ID: sea-83505

Subject(s)
Child , Homocystinuria/diagnosis , Humans , Male , Mass Screening , Intellectual Disability/metabolism
13.
Biochemical investigations in five patients with phenylketonuria.
Rao, B S; Narayanan, H S; Reddy, G N.
Article in English | IMSEAR | ID: sea-22211

Subject(s)
Child , Child, Preschool , Female , Humans , India , Male , Molecular Biology , Phenylalanine/blood , Phenylketonurias/genetics
14.
Phenylketonuria--report of a case.
Rao, B S; Narayanan, H S; Nataraj, C L.
Indian Pediatr ; 1970 Jan; 7(1): 58-60
Article in English | IMSEAR | ID: sea-13622

Subject(s)
Chemical Phenomena , Chemistry , Child , Chromatography , Female , Humans , India , Male , Methods , Pedigree , Phenylalanine/blood , Phenylketonurias/epidemiology
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