Search | Global Index Medicus

1.

Parahydroxyphenylpyruvicacidemia in tyrosinosis.

Jaiswal, R B; Bhai, I; Daginawala, H F; Nath, N; Nath, M C.

Indian Pediatr ; 1978 Nov; 15(11): 893-9

Article in English | IMSEAR | ID: sea-11638

Subject(s)

4-Hydroxyphenylpyruvate Dioxygenase/deficiency , Adolescent , Adult , Amino Acid Metabolism, Inborn Errors/blood , Child , Female , Humans , Liver/enzymology , Male , Phenylpyruvic Acids/blood , Tyrosine/blood , Tyrosine Transaminase/deficiency

2.

Screening tests in hypertriglyceridemia thalassemia syndrome.

Parande, C M; Wechalekar, M D; Bhai, I; Parande, A S; Jaiswal, R B.

Indian Pediatr ; 1975 Jul; 12(7): 593-8

Article in English | IMSEAR | ID: sea-12956

Subject(s)

Child, Preschool , Humans , Hyperlipidemias/diagnosis , Infant , Syndrome , Thalassemia/diagnosis , Triglycerides/blood

3.

Tyrosinosis (tyrosinaemia).

Jaiswal, R B.

Indian Pediatr ; 1975 Mar; 12(3): 209-10

Article in English | IMSEAR | ID: sea-16017

Subject(s)

4-Hydroxyphenylpyruvate Dioxygenase/metabolism , Amino Acid Metabolism, Inborn Errors/enzymology , Humans , Liver/enzymology , Middle Aged , Oxygenases/metabolism , Tyrosine/metabolism , Tyrosine Transaminase/metabolism

4.

Hypertriglyceridemia-thalassemia syndrome.

Jaiswal, R B; Bhai, I; Parande, A S; Wechalekar, M D; Nath, M C.

Indian Pediatr ; 1974 May; 11(5): 385-9

Article in English | IMSEAR | ID: sea-7857

Subject(s)

Adolescent , Adult , Child , Child, Preschool , Female , Humans , Hyperlipidemias/genetics , Infant , Male , Syndrome , Thalassemia/genetics , Triglycerides/blood

5.

Tyrosinosis. I. Clinical, radiological and biochemical aspects.

Jaiswal, R B; Bhai, I; Nath, N; Nath, M C.

Indian Pediatr ; 1969 Jan; 6(1): 1-17

Article in English | IMSEAR | ID: sea-14321

Subject(s)

Adolescent , Adult , Amino Acid Metabolism, Inborn Errors , Amino Acids/urine , Blood Proteins/analysis , Child , Child, Preschool , Chromatography , Female , Humans , Infant , Male , Phosphates/urine , Tyrosine/metabolism

6.

Chromosomal abnormalities in measles.

Grover, S; Solanki, B K; Khandelwal, M K; Jaiswal, R B.

Indian Pediatr ; 1968 Jul; 5(7): 326-9

Article in English | IMSEAR | ID: sea-11965

Subject(s)

Adult , Child , Child, Preschool , Chromosome Aberrations , Chromosome Disorders , Female , Humans , Infant , Karyotyping , Male , Measles/genetics

7.

Hereditary methaemoglobinaemia: case report of congenital cyanosis in a Rajput child.

Jaiswal, R B; Khandelwal, M K; Tiwaskar, H V.

Indian Pediatr ; 1968 May; 5(5): 226-9

Article in English | IMSEAR | ID: sea-7900

Subject(s)

Child, Preschool , Cyanosis/congenital , Humans , India , Male , Methemoglobinemia/genetics

8.

Chromosomal analysis in some cases of mental and physical defects in children.

Khandelwal, M K; Jaiswal, R B; Solanki, B R; Grover, S.

Indian Pediatr ; 1968 Mar; 5(3): 100-6

Article in English | IMSEAR | ID: sea-7160

Subject(s)

Bone and Bones/abnormalities , Child , Child, Preschool , Chromosome Aberrations , Chromosome Disorders , Down Syndrome , Female , Heart Defects, Congenital/genetics , Humans , Karyotyping , Male , Intellectual Disability/genetics

9.

Pick-Niemann's disease. Case report in an Indian Punjabi child.

Jaiswal, R B; Khandelwal, M K; Solanki, B R; Parande, A S.

Indian Pediatr ; 1967 Nov; 4(11): 418-21

Article in English | IMSEAR | ID: sea-14237

Subject(s)

Female , Humans , India , Infant , Niemann-Pick Diseases/epidemiology

10.

Acute lymphatic leukaemia: report of case.

Jaiswal, R B; Patoria, N K; Khandelwal, M.

Indian Pediatr ; 1965 Nov; 2(11): 419-21

Article in English | IMSEAR | ID: sea-12420

Subject(s)

Child, Preschool , Humans , Leukemia, Lymphoid , Male

11.

Infantile cortical hyperostosis: report of a case.

Jaiswal, R B; Knandelwal, M; Patoria, N K.

Indian Pediatr ; 1965 May; 2(5): 181-4

Article in English | IMSEAR | ID: sea-15569

Subject(s)

Humans , Hyperostosis, Cortical, Congenital/diagnosis , Infant , Prednisolone/therapeutic use , Radiography

12.

EPIDERMOLYSIS BULLOSA DYSTROPHICA: REPORT OF A CASE.

JAISWAL, R B; KHANDELWAL, M K; PARANJAPE, S; SOLANKI, B R; PATORIA, N K.

Indian Pediatr ; 1964 Dec; 1(): 493-7

Article in English | IMSEAR | ID: sea-12261

Subject(s)

Epidermolysis Bullosa , Genetics, Medical , Infant , Mouth Diseases , Pathology

13.

CONGENITAL EPIDERMOLYSIS BULLOSA SIMPLEX.

JAISWAL, R B.

Indian Pediatr ; 1964 Jun; 1(): 237-9

Article in English | IMSEAR | ID: sea-9879

Subject(s)

Anti-Bacterial Agents , Epidermolysis Bullosa , Genetics, Medical , India , Infant, Newborn , Infant, Newborn, Diseases , Pathology

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