Pages that link to "Q57390264"
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The following pages link to Risk of developing a mitochondrial DNA deletion disorder (Q57390264):
Displaying 50 items.
- Mitochondrial DNA mutations in human disease (Q24676881) (← links)
- Leber hereditary optic neuropathy: current perspectives (Q26863599) (← links)
- Mitochondrial DNA disease and developmental implications for reproductive strategies (Q28649392) (← links)
- Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management (Q30459704) (← links)
- Transmission of mitochondrial DNA diseases and ways to prevent them. (Q33658696) (← links)
- High rate of large deletions in Caenorhabditis briggsae mitochondrial genome mutation processes (Q33730934) (← links)
- A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO). (Q33737397) (← links)
- De novo mtDNA point mutations are common and have a low recurrence risk. (Q33886230) (← links)
- Therapeutic prospects for mitochondrial disease (Q34205124) (← links)
- The neuro-ophthalmology of mitochondrial disease (Q34338783) (← links)
- Gene therapy for the treatment of mitochondrial DNA disorders (Q34401459) (← links)
- Mitochondrial disease (Q34543745) (← links)
- Novel mitochondrial tRNA(Ile) m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype (Q35208474) (← links)
- Mitochondrial energetics and therapeutics (Q35632864) (← links)
- Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes. (Q35795439) (← links)
- Mitochondrial DNA and disease (Q36194900) (← links)
- Deletion-mutant mtDNA increases in somatic tissues but decreases in female germ cells with age. (Q36416150) (← links)
- Mitochondrial disease: genetics and management (Q36492283) (← links)
- Extraocular mitochondrial myopathies and their differential diagnoses (Q36499611) (← links)
- Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease (Q36532577) (← links)
- Diagnosis and treatment of mitochondrial myopathies (Q36634939) (← links)
- Mitochondrial DNA and the mammalian oocyte. (Q36707790) (← links)
- Mitochondria as a target of environmental toxicants (Q36956066) (← links)
- Three families with 'de novo' m.3243A > G mutation (Q36987749) (← links)
- Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders (Q37023068) (← links)
- The advances and new technologies for the study of mitochondrial diseases (Q37091059) (← links)
- What causes mitochondrial DNA deletions in human cells? (Q37096545) (← links)
- The inheritance of pathogenic mitochondrial DNA mutations (Q37419954) (← links)
- The genetics and pathology of mitochondrial disease. (Q37560946) (← links)
- The clinical maze of mitochondrial neurology (Q37648911) (← links)
- Antenatal manifestations of mitochondrial disorders. (Q38077672) (← links)
- mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal development (Q38293604) (← links)
- Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosis (Q38574817) (← links)
- Genetic Counselling for Maternally Inherited Mitochondrial Disorders. (Q39325696) (← links)
- Transmission of mitochondrial DNA disorders: possibilities for the future. (Q40310646) (← links)
- Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report (Q41968641) (← links)
- Aging, Metabolism, and Cancer Development: from Peto's Paradox to the Warburg Effect (Q42364240) (← links)
- Mitochondrial diseases: molecular mechanisms, clinical presentations and diagnosis investigations (Q46835436) (← links)
- Sources, mechanisms, and consequences of chemical-induced mitochondrial toxicity. (Q47131435) (← links)
- Older mothers are not at risk of having grandchildren with sporadic mtDNA deletions (Q48195887) (← links)
- Mitochondrial DNA deletion in a child with mitochondrial encephalomyopathy, growth hormone deficiency, and hypoparathyroidism. (Q48376079) (← links)
- Clinical evolution of Kearns-Sayre syndrome with polyendocrinopathy and respiratory failure (Q48472389) (← links)
- Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy (Q49711797) (← links)
- The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease (Q50994607) (← links)
- Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells (Q56349520) (← links)
- mtDNA single macrodeletions associated with myopathies: Absence of haplogroup-related increased risk (Q57688185) (← links)
- A new POLG1 mutation with peo and severe axonal and demyelinating sensory–motor neuropathy (Q58052165) (← links)
- [Diagnostic investigations of mitochondrial diseases with neurological symptoms] (Q79918878) (← links)
- Electron microscopic findings in levator muscle biopsies of patients with isolated congenital or acquired ptosis (Q80377130) (← links)
- Mitochondrial encephalomyopathies (Q82029875) (← links)