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1.

Sphingolipid errors in mentally retarded south Indian children--II.

Joshua, G E; Mokashi, S; Bhaktaviziam, A.

Article in English | IMSEAR | ID: sea-24271

Subject(s)

Brain/pathology , Brain Chemistry , Child , Child, Preschool , Female , Humans , India , Lipidoses/metabolism , Male

2.

Sphingolipid errors in mentally retarded south Indian children--I.

Joshua, G E; Basu, D K; Mathai, K V.

Article in English | IMSEAR | ID: sea-23462

Subject(s)

Brain/pathology , Brain Chemistry , Child , Child, Preschool , Female , Humans , India , Infant , Male , Sphingolipidoses/metabolism

3.

The genetic component in mentally retarded South Indian children.

Joshua, G E.

Article in English | IMSEAR | ID: sea-23822

Subject(s)

Brain Diseases/complications , Child , Child, Preschool , Consanguinity , Female , Humans , India , Infant , Male , Intellectual Disability/etiology , Metabolism, Inborn Errors/complications

4.

Mental retardation in children. III. Tay-Sachs disease and infantile lipid storage disorders with visceral involvement.

Joshua, G E; Bhaktaviziam, A; Bala, V I.

Indian Pediatr ; 1974 May; 11(5): 369-76

Article in English | IMSEAR | ID: sea-15136

Subject(s)

Brain Chemistry , Child, Preschool , Female , Humans , Infant , Liver/pathology , Male , Sphingolipidoses/metabolism , Sphingolipids/analysis , Spleen/pathology

5.

GM1 gangliosidosis in a South Indian child--a clinico-pathological and biochemical study.

Joshua, G E; Bhaktaviziam, A; Sudarazanam, D; Basu, D K.

Article in English | IMSEAR | ID: sea-17412

Subject(s)

Autopsy , Brain/pathology , Brain Chemistry , Gangliosides/analysis , Humans , Infant , Lipid Metabolism, Inborn Errors/metabolism , Male

6.

Mental retardation in children. II. Leucodystrophies.

Joshua, G E; Jadhav, M; Bhaktaviziam, A; Mokashi, S.

Indian Pediatr ; 1974 Jan; 11(1): 53-9

Article in English | IMSEAR | ID: sea-11235

Subject(s)

Brain Chemistry , Child , Child, Preschool , Diffuse Cerebral Sclerosis of Schilder/enzymology , Female , Frontal Lobe/pathology , Humans , Infant , Male , Sphingolipids/analysis , Syndrome

7.

Mental retardation in children. I. An etiological study of 303 cases.

Joshua, G E.

Indian Pediatr ; 1974 Jan; 11(1): 47-51

Article in English | IMSEAR | ID: sea-10897

Subject(s)

Birth Injuries/complications , Child , Child, Preschool , Congenital Abnormalities/complications , Encephalitis/complications , Female , Humans , India , Infant , Male , Meningitis/complications , Intellectual Disability/etiology , Metabolism, Inborn Errors/complications , Pilot Projects

8.

Hepatolenticular degeneration (Wilson's disease) and rickets in children.

Joshua, G E.

Article in English | IMSEAR | ID: sea-17570

Subject(s)

Child , Electroencephalography , Female , Hepatolenticular Degeneration/complications , Humans , Kidney Diseases/etiology , Male , Rickets/etiology

9.

Juvenile heredo familial lipidosis (Spielmeyer-Vogt): an electron microscopic study.

Joshua, G E; Bhaktaviziam, A; Job, C K; Basu, D K.

Article in English | IMSEAR | ID: sea-16302

Subject(s)

Child , Frontal Lobe/pathology , Humans , Lipidoses/genetics , Male , Microscopy, Electron , Neurons

10.

Phenylketonuria in Tamilnadu (South India).

Joshua, G E; Nair, N G; Radhakrishnan, A N.

Indian Pediatr ; 1973 Apr; 10(4): 245-52

Article in English | IMSEAR | ID: sea-10535

Subject(s)

Child, Preschool , Electroencephalography , Female , Humans , India , Infant , Pedigree , Phenylketonurias/diagnosis

11.

Subacute sclerosing panencephalitis: a clinico-pathological report including the biochemical findings of abnormal ganglioside pattern in the brain of a case of subacute inclusion body encephalitis.

Joshua, G E; Bhaktaviziam, A; Kokrady, S; Mathai, K V.

Article in English | IMSEAR | ID: sea-26099

Subject(s)

Autopsy , Brain/pathology , Brain Chemistry , Child , Chromatography, Thin Layer , Gangliosides/analysis , Humans , Male , Subacute Sclerosing Panencephalitis/metabolism

12.

Heredo-familial lipidosis-juvenile (Spielmeyer-Vogt) and late infantile (Bielschowsky) forms. A biochemical study.

Joshua, G E; Kokrady, S; Mathai, K V.

Neurol India ; 1971 Dec; 19(4): 181-7

Article in English | IMSEAR | ID: sea-120590

Subject(s)

Biopsy , Brain/metabolism , Child , Diagnosis, Differential , Female , Gangliosides/metabolism , Histocytochemistry , Humans , Lipid Metabolism, Inborn Errors/metabolism , Lipidoses/metabolism

13.

Lead poisoning in a family of 18 members in Vellore town.

Joshua, G E; Ratnaike, N; Benjamin, V.

Article in English | IMSEAR | ID: sea-16703

Subject(s)

Adolescent , Adult , Child , Child, Preschool , Chronic Disease , Female , Humans , India , Industrial Waste , Infant , Infant, Newborn , Lead/blood , Lead Poisoning/diagnosis , Male , Middle Aged , Porphyrins/urine

14.

Cerebro-retinal degeneration. Clinical and histopathological study.

Joshua, G E; Bhakthaviziam, A; Jadhav, M; Mathai, K V.

Indian Pediatr ; 1970 Aug; 7(8): 418-28

Article in English | IMSEAR | ID: sea-10651

Subject(s)

Adolescent , Brain/pathology , Child , Child, Preschool , Consanguinity , Electroencephalography , Female , Fundus Oculi , Humans , Lipidoses/pathology , Pedigree , Retinal Degeneration/genetics

15.

Chronic lead poisoning: recurrent encephalopathy in a child.

Joshua, G E.

Indian Pediatr ; 1969 May; 6(5): 329-37

Article in English | IMSEAR | ID: sea-10586

Subject(s)

Accidents, Home , Adult , Brain Diseases/chemically induced , Chronic Disease , Female , Humans , India , Infant , Lead Poisoning

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