Pages that link to "Q93657316"
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The following pages link to The retinal manifestations of mitochondrial myopathy. A study of 22 cases (Q93657316):
Displaying 23 items.
- The significance of opthalmologic evaluation in the early diagnosis of inborn errors of metabolism: the Cretan experience (Q24806852) (← links)
- Mitochondrial disease in childhood: nuclear encoded (Q26820866) (← links)
- Cone and rod dysfunction in the NARP syndrome (Q28139048) (← links)
- Adaptive optics scanning laser ophthalmoscopy images in a family with the mitochondrial DNA T8993C mutation (Q30853128) (← links)
- Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder (Q33672801) (← links)
- Risk factors of ocular involvement in children with mitochondrial respiratory chain complex defect. (Q34494711) (← links)
- Management of myogenic ptosis (Q34621939) (← links)
- A new mitochondrial disease associated with mitochondrial DNA heteroplasmy (Q34627393) (← links)
- Differentiating idiopathic inflammatory myopathies from metabolic myopathies (Q35036173) (← links)
- Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence (Q36940979) (← links)
- Retinitis pigmentosa, ataxia, and mental retardation associated with mitochondrial DNA mutation in an Italian family (Q37299771) (← links)
- Vitelliform macular degeneration associated with mitochondrial myopathy (Q39686143) (← links)
- Aplasia of the retinal vessels combined with optic nerve hypoplasia, neonatal epileptic seizures, and lactic acidosis due to mitochondrial complex I deficiency (Q41930287) (← links)
- Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy (Q44028130) (← links)
- Ophthalmologic findings in patients with ataxia (Q46155985) (← links)
- Macular pattern dystrophy associated with a mutation of mitochondrial DNA. (Q50518875) (← links)
- Progressive External Ophthalmoplegia. (Q53924716) (← links)
- Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNALeu A to G mutation11The authors have no proprietary interest in the development or marketing of any device or medica (Q57943560) (← links)
- Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness (Q60609066) (← links)
- Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation. (Q64979218) (← links)
- Mitochondrial encephalomyopathies (Q70244859) (← links)
- Mitochondrial disorders and ataxia (Q79341034) (← links)
- [Diabetes and mitochondrial cytopathies: pathological studies] (Q81573384) (← links)