(Q44761373)

6 December 2017

Mitochondrial mutation in Iranian patients with multiple sclerosis, correlation between haplogroups H, A and clinical manifestations (English)

1 reference

6 December 2017

0 references

Mohammad Hossein Sanati

object named as

Mohammad Hossein Sanati

7

0 references

Mohammad Ali Sahraian

object named as

Mohammad Ali Sahraian

5

0 references

Alipasha Meysamie

4

object named as

Alipasha Meysamie

1 reference

6 December 2017

6

Asghar Bayati

1 reference

6 December 2017

9

Homa Sadeghian

1 reference

6 December 2017

1

Mojdeh Ghabaee

1 reference

6 December 2017

Motahar Omranisikaroudi

2

1 reference

6 December 2017

Shahla Amrisaroukolaei

3

1 reference

6 December 2017

Mossoud Houshman

8

1 reference

6 December 2017

Khalili Vajihazaman

10

1 reference

6 December 2017

14 November 2008

1 reference

Cellular and Molecular Neurobiology

6 December 2017

1 reference

6 December 2017

29

1 reference

6 December 2017

3

1 reference

6 December 2017

341-346

1 reference

https://scigraph.springernature.com/pub.10.1007/s10571-008-9325-7

6 December 2017

0 references

cites work

Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10571-008-9325-7

Anticipation of age at onset in multiple sclerosis: a Sardinian cohort study

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10571-008-9325-7

Clinical concordance in sibling pairs with multiple sclerosis.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10571-008-9325-7

New insights into the immunogenetics of multiple sclerosis.

21 January 2018

1 reference

12 December 2020

Sequence and organization of the human mitochondrial genome

1 reference

12 December 2020

Offspring recurrence rates and clinical characteristics of conjugal multiple sclerosis

1 reference

12 December 2020

Comparison of clinical and demographic features between affected pairs of Italian multiple sclerosis multiplex families; relation to tumour necrosis factor genomic polymorphisms.

1 reference

12 December 2020

Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement

1 reference

12 December 2020

An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy

1 reference

12 December 2020

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS

1 reference

12 December 2020

mtDNA haplogroup J: a contributing factor of optic neuritis

1 reference

12 December 2020

Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.

1 reference

12 December 2020

Mitochondrial haplogroups in Basque multiple sclerosis patients

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis

1 reference

12 December 2020

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

1 reference

12 December 2020

Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.

1 reference

12 December 2020

A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

1 reference

12 December 2020

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

12 December 2020

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

1 reference

12 December 2020

Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis

1 reference

12 December 2020

Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis

1 reference

12 December 2020

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees

1 reference

12 December 2020

10.1007/S10571-008-9325-7

Identifiers

DOI

1 reference

6 December 2017

1 reference