Cargando…

Mitochondrial disorders: Challenges in diagnosis & treatment

Mitochondrial dysfunctions are known to be responsible for a number of heterogenous clinical presentations with multi-systemic involvement. Impaired oxidative phosphorylation leading to a decrease in cellular energy (ATP) production is the most important cause underlying these disorders. Despite sig...

Descripción completa

Detalles Bibliográficos
Autores principales:	Khan, Nahid Akhtar, Govindaraj, Periyasamy, Meena, Angamuthu Kannan, Thangaraj, Kumarasamy
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2015
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405934/ https://www.ncbi.nlm.nih.gov/pubmed/25857492

Ejemplares similares

Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy
por: Khan, Nahid Akhtar, et al.
Publicado: (2013)

Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures
por: Paramasivam, Arumugam, et al.
Publicado: (2020)

Correction to: Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures
por: Paramasivam, Arumugam, et al.
Publicado: (2020)

Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
por: Chakrabarty, Sanjiban, et al.
Publicado: (2021)

Vocal cord palsy in a case of chronic progressive external ophthalmoplegia
por: Ramakrishnan, Subasree, et al.
Publicado: (2015)

Genomic view on the peopling of India
por: Tamang, Rakesh, et al.
Publicado: (2012)

The Epigenetic Role of miR-124 in HIV-1 Tat- and Cocaine-Mediated Microglial Activation
por: Periyasamy, Palsamy, et al.
Publicado: (2022)

Severe acute respiratory syndrome coronaviruses contributing to mitochondrial dysfunction: Implications for post-COVID complications
por: Prasada Kabekkodu, Shama, et al.
Publicado: (2023)

Complete mitochondrial genome sequence of Asiatic lion (Panthera leo persica)
por: Tabasum, Wajeeda, et al.
Publicado: (2016)

Congenital muscular dystrophy with inflammation: Diagnostic considerations
por: Konkay, Kaumudi, et al.
Publicado: (2016)

Challenges in the diagnosis and treatment of pediatric obsessive–compulsive disorder
por: Westwell-Roper, Clara, et al.
Publicado: (2019)

In situ origin of deep rooting lineages of mitochondrial Macrohaplogroup 'M' in India
por: Thangaraj, Kumarasamy, et al.
Publicado: (2006)

Comparison of high-resolution sonography and electrophysiology in the diagnosis of carpal tunnel syndrome
por: Kanikannan, Meena Angamuthu, et al.
Publicado: (2015)

The Challenges in Diagnosis and Treatment of Dissociative Disorders
por: Chien, Wai Tong, et al.
Publicado: (2022)

Diagnosis and Treatment of Mitochondrial Myopathies
por: Ahmed, Syeda T., et al.
Publicado: (2018)

Mitochondrial Genetic Heterogeneity in Leber’s Hereditary Optic Neuropathy: Original Study with Meta-Analysis
por: Jha, Rajan Kumar, et al.
Publicado: (2021)

A novel insertion-induced frameshift mutation of the androgen receptor gene in a patient with primary amenorrhea()
por: Sharma, Vikas, et al.
Publicado: (2013)

Diagnosis and treatment of mitochondrial myopathies
por: Pfeffer, Gerald, et al.
Publicado: (2013)

Cellular and Molecular Evidence of Multiple Sclerosis Diagnosis and Treatment Challenges
por: Khan, Zuber, et al.
Publicado: (2023)

Pregnancy and pituitary disorders: Challenges in diagnosis and management
por: Laway, Bashir A., et al.
Publicado: (2013)

HIV TAT-mediated microglial senescence: Role of SIRT3-dependent mitochondrial oxidative stress
por: Thangaraj, Annadurai, et al.
Publicado: (2020)

Mitochondrial Fatty Acid Oxidation Disorders: Laboratory Diagnosis, Pathogenesis, and the Complicated Route to Treatment
por: Wanders, Ronald J.A., et al.
Publicado: (2020)

Retinoblastoma discordance in families with twins
por: Abraham, Aloysius, et al.
Publicado: (2019)

Genetic affinities among the lower castes and tribal groups of India: inference from Y chromosome and mitochondrial DNA
por: Thanseem, Ismail, et al.
Publicado: (2006)

Biochemical diagnosis of mitochondrial disorders
por: Rodenburg, Richard J. T.
Publicado: (2010)

Ototoxicity: A Challenge in Diagnosis and Treatment
por: Ganesan, Purushothaman, et al.
Publicado: (2018)

Sleep Disordered Breathing challenges: From diagnosis to treatment
por: Lorenzi Filho, Geraldo, et al.
Publicado: (2018)

Challenges in the diagnosis and treatment of CNS demyelinating disorders in Zambia
por: Miskin, Dhanashri P, et al.
Publicado: (2016)

Glucose Metabolism Disorders: Challenges and Opportunities for Diagnosis and Treatment
por: Vekic, Jelena, et al.
Publicado: (2022)

Challenges in the diagnosis & treatment of miliary tuberculosis
por: Sharma, Surendra K., et al.
Publicado: (2012)

Heterogeneity in Hematological Parameters of High and Low Altitude Tibetan Populations
por: Basak, Nipa, et al.
Publicado: (2021)

Global Patterns in Human Mitochondrial DNA and Y-Chromosome Variation Caused by Spatial Instability of the Local Cultural Processes
por: Kumar, Vikrant, et al.
Publicado: (2006)

Role of Autophagy in HIV-1 and Drug Abuse-Mediated Neuroinflammaging
por: Sil, Susmita, et al.
Publicado: (2022)

Pulmonary Aspergillosis: An Evolving Challenge for Diagnosis and Treatment
por: Russo, Alessandro, et al.
Publicado: (2020)

Challenges in the Diagnosis and Individualized Treatment of Cervical Cancer
por: Schubert, Melanie, et al.
Publicado: (2023)

Review of Technological Challenges in Personalised Medicine and Early Diagnosis of Neurodegenerative Disorders
por: Domínguez-Fernández, Celtia, et al.
Publicado: (2023)

Pinpointing the Geographic Origin of 165-Year-Old Human Skeletal Remains Found in Punjab, India: Evidence From Mitochondrial DNA and Stable Isotope Analysis
por: Sehrawat, J.S., et al.
Publicado: (2022)

Correction: Global Patterns in Human Mitochondrial DNA and Y-Chromosome Variation Caused by Spatial Instability of the Local Cultural Processes
por: Kumar, Vikrant, et al.
Publicado: (2006)

Diabetic Nephropathy: Challenges in Pathogenesis, Diagnosis, and Treatment
por: Samsu, Nur
Publicado: (2021)

Application of High Throughput Technologies in the Development of Acute Myeloid Leukemia Therapy: Challenges and Progress
por: Xiang, Wei, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_cvbt09ip107cf7d31ib56orth6