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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

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

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

CONGENITAL HYPOPLASTIC ANAEMIA. FURTHER OBSERVATIONS ON A PREVIOUSLY REPORTED CASE.

PARANDE, A S; JAIN, K L.

Article in English | IMSEAR | ID: sea-93136

Subject(s)

Amino Acid Metabolism, Inborn Errors , Anemia, Aplastic , ortho-Aminobenzoates , Infant , Urine

CONGENITAL HYPOPLASTIC ANAEMIA: A CASE REPORT.

PARANDE, A S; JAIN, K L.

Article in English | IMSEAR | ID: sea-85353

Subject(s)

Anemia, Aplastic , Genetics, Medical , Hemoglobinometry , Infant , Prednisone

Congenital afibrinogenemia (a case report).

JAIN, K L; PARANDE, A S.

Article in English | IMSEAR | ID: sea-93438

Subject(s)

Afibrinogenemia

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