(Q39160975)

9 September 2017

Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria (English)

1 reference

9 September 2017

1 reference

A Larnaout

1

1 reference

9 September 2017

F Hentati

2

1 reference

9 September 2017

S Belal

3

1 reference

9 September 2017

C Ben Hamida

4

1 reference

9 September 2017

N Kaabachi

5

1 reference

9 September 2017

M Ben Hamida

6

1 reference

9 September 2017

1 January 1994

1 reference

9 September 2017

Acta Neuropathologica

1 reference

9 September 2017

88

1 reference

9 September 2017

367-370

1 reference

9 September 2017

4

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00310381

9 September 2017

0 references

cites work

Agenesis of the corpus callosum and gyral malformations are frequent manifestations of nonketotic hyperglycinemia

1 reference

12 December 2020

L-2-hydroxyglutaric acidemia: A novel inherited neurometabolic disease

1 reference

12 December 2020

Hypothesis: a role for quinolinic acid in the neuropathology of glutaric aciduria type I.

1 reference

12 December 2020

Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change

1 reference

12 December 2020

L-2-Hydroxyglutaric aciduria: an inborn error of metabolism?

1 reference

12 December 2020

Hereditary hyperammonaemia

1 reference

12 December 2020

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis.

1 reference

12 December 2020

Inhibition of brain glutamate decarboxylase by glutarate, glutaconate, and β-Hydroxyglutarate: Explanation of the symptoms in glutaric aciduria?

1 reference

12 December 2020

Leigh's disease--several nosological entities with an identical histopathological complex?

1 reference

12 December 2020

Cortical subacute necrotizing encephalomyelopathy. A study of two patients with mitochondrial dysfunction.

1 reference

12 December 2020

Ornithine carbamoyl transferase deficiency: a neuropathological study

1 reference

12 December 2020

Glutaric acidemia: a metabolic disorder causing progressive choreoathetosis

1 reference

12 December 2020

Morphologic and histoanatomic observations of the brain in untreated human phenylketonuria.

1 reference

12 December 2020

Familial encephalopathy and L-2-hydroxyglutaric aciduria

1 reference

12 December 2020

A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00310381

1 reference

9 September 2017

1 reference