(Q44551833)

4 December 2017

Liver disease in Navajo neuropathy (English)

1 reference

4 December 2017

1 reference

Holve S

1

1 reference

4 December 2017

Hu D

2

1 reference

4 December 2017

Shub M

3

1 reference

4 December 2017

Tyson RW

4

1 reference

4 December 2017

Sokol RJ

5

1 reference

4 December 2017

language of work or name

English

0 references

publication date

1 October 1999

1 reference

The Journal of Pediatrics

4 December 2017

1 reference

4 December 2017

135

1 reference

4 December 2017

4

1 reference

4 December 2017

482-493

1 reference

Acromutilating, Paralyzing Neuropathy With Corneal Ulceration in Navajo Children

4 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Neuropathy in Navajo children: clinical and epidemiologic features

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Metachromatic leukodystrophy in the Navajo Indian population: a splice site mutation in intron 4 of the arylsulfatase A gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Neuropsychological deficits and morphological MRI brain scan abnormalities in apparently healthy non-encephalopathic patients with cirrhosis. A controlled study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Prospective study of children with alpha 1-antitrypsin deficiency: eight-year-old follow-up

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

High prevalence of viral infection in adults with homozygous and heterozygous alpha 1-antitrypsin deficiency and chronic liver disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Liver involvement in Alpers disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

Disorders of the mitochondria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2899%2970172-1

10.1016/S0022-3476(99)70172-1

7 January 2021

Identifiers

DOI

1 reference

4 December 2017

1 reference