Atf3 controls transitioning in female mitochondrial cardiomyopathy as identified by spatial and single-cell transcriptomics.
Journal: Science advances
Year: April 04, 2025
Geneticist
5
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Leigh Syndrome
Mitochondrial Complex 1 Deficiency
Sengers Syndrome
Coenzyme Q Cytochrome C Reductase Deficiency
Cytochrome C Oxidase Deficiency
Holocarboxylase Synthetase Deficiency
Lactic Acidosis
Mohr-Tranebjaerg Syndrome
Multiple Carboxylase Deficiency
Perrault Syndrome
Sideroblastic Anemia
Alpers-Huttenlocher Syndrome
Alternating Hemiplegia of Childhood
Anemia
CACH Syndrome
Cardiomyopathy
Cerebellar Hypoplasia
Congenital Cataract
Diabetic Ketoacidosis
Diabetic Nephropathy
Drug Induced Dyskinesia
Epilepsy
Epilepsy in Children
Hearing Loss
Hemiplegia
Hereditary Ataxia
Hypotonia
Infant Respiratory Distress Syndrome
Infantile Axonal Neuropathy
Intersex
Leukodystrophy
Liver Failure
MELAS Syndrome
Metabolic Acidosis
Mitochondrial Neurogastrointestinal Encephalopathy Disease
Optic Nerve Atrophy
Pelizaeus-Merzbacher Disease
Peripheral Neuropathy
Premature Ovarian Failure
Seizures
Short Stature (Growth Disorders)
Tissue Biopsy
Tumefactive Multiple Sclerosis
Turner Syndrome
Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
West Syndrome
Wilson Disease
David R. Thorburn is a male healthcare professional who helps patients with various health conditions like Leigh Syndrome, epilepsy, hearing loss, and more. He is skilled in diagnosing and treating complex medical issues related to metabolism, genetics, and neurology.
Patients trust David R. Thorburn because he communicates clearly and compassionately. He listens to their concerns, explains treatment options in simple terms, and involves them in decision-making.
To stay updated with the latest medical knowledge, David R. Thorburn regularly attends conferences, reads research articles, and collaborates with other experts in the field. This helps him provide the best possible care to his patients.
David R. Thorburn works closely with colleagues and other healthcare professionals to ensure a coordinated approach to patient care. By sharing knowledge and expertise, they collectively strive to improve patient outcomes and experiences.
Through his dedication and expertise, David R. Thorburn has positively impacted many patients' lives. His research on mitochondrial cardiomyopathy, as published in "Atf3 controls transitioning in female mitochondrial cardiomyopathy as identified by spatial and single-cell transcriptomics," has contributed valuable insights to the medical community.
In conclusion, David R. Thorburn is a caring and knowledgeable healthcare provider who goes above and beyond to help his patients. His commitment to ongoing learning, collaboration with colleagues, and groundbreaking research work make him a trusted and respected figure in the medical field.
Journal: Science advances
Year: April 04, 2025
David R. Thorburn is an amazing Geneticist in Melbourne. He was so kind and explained everything clearly. I felt really comfortable during my appointment. Highly recommend!
Dr. Thorburn is a fantastic Geneticist. He helped me understand my genetic condition in a way that was easy to grasp. His expertise and care are truly commendable.
I had a great experience with David R. Thorburn as my Geneticist. He was very patient and answered all my questions. I left feeling reassured and well-informed. Thank you!
Dr. Thorburn is a top-notch Geneticist. He is not only knowledgeable but also very compassionate. I appreciate the time he took to listen to my concerns and provide personalized care.
I highly recommend David R. Thorburn as a Geneticist in Melbourne. He is truly dedicated to his patients and goes above and beyond to ensure they receive the best care possible. Thank you for everything!