The 20 Best Carnitine Palmitoyltransferase 1 Deficiency Doctors Near Me in Michigan, US

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 8 years. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics, American Board Of Medical Genetics And Genomics, and American Board Of Pediatrics.

Linda Rossetti is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 10 years. Dr. Rossetti is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 87 other conditions, according to our data. Her clinical expertise encompasses Smith-Magenis Syndrome, Miller-Dieker Syndrome, Chromosome 6q Duplication, and Chromosome 8p Deletion. Dr. Rossetti is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Nicki Cain is a Pediatrics provider practicing medicine in Caledonia, Michigan. She has been practicing medicine for over 18 years. Dr. Cain is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Obesity in Children, Croup, Herpangina, and Carnitine Palmitoyltransferase 2 Deficiency. Dr. Cain is board certified in American Board Of Pediatrics. Dr. Cain is currently accepting new patients.

Dr. Pritchard is a Michigan native who returned to the University of Michigan to join the faculty here in 2019 after completing her pediatrics and genetics residencies and biochemical genetics fellowship. She enjoys care of complex patients with rare genetic diseases. Dr. Pritchard is active in medical education as Program Director for the Medical Biochemical Genetics Fellowship program and Associate Program Director for the Medical Genetics and Genomics training programs.Outside of work, Dr. Pritchard enjoys cooking, reading, hiking, and spending time with her husband and two daughters. Dr. Pritchard is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 149 other conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Cohen Syndrome.

Dr. DiMagno grew up in southern Illinois and completed her undergraduate studies in Biology at Washington University in St. Louis. She earned her medical degree from the University of Illinois at Chicago and completed her Internal Medicine residency at the University of Michigan in 1998. She is board certified in Internal Medicine.She joined the faculty at Michigan Medicine in 1998 and spent 20 years practicing Primary Care General Internal Medicine at the Brighton Health Center. In 2018, she became part of the founding team of the newly opened Victors Care program, where she continues to provide personalized, relationship-based care. She was appointed Medical Director in 2021.Her clinical interests include patient-physician communication, preventive care, women’s health, and behavior change in chronic disease. A longtime educator of medical students and residents, Dr. DiMagno brings that experience into her practice through clear communication and shared decision-making. She emphasizes personalized, evidence-informed care grounded in trust, continuity, and a desire to understand each patient’s values and goals.She and her husband, Matthew, have four children, now ranging from middle school through college. Much of her free time is spent cheering them on from the sidelines of hockey, soccer, and lacrosse—hockey remains her favorite. She has played recreational hockey since her daughter first took up the sport and continues to enjoy the game. She also enjoys supporting her children’s musical performances and spending time outdoors and with family. Dr. Dimagno is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Carnitine Palmitoyltransferase 2 Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, Bloom Syndrome, and Urticaria Pigmentosa. Dr. Dimagno is board certified in Internal Medicine.

Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as an Advanced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 50 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics.

Ximena Arcila is a Neurologist practicing medicine in West Bloomfield, Michigan. Dr. Arcila is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 17 other conditions, according to our data. Her clinical expertise encompasses Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease), Spinal Muscular Atrophy (SMA), Spinal and Bulbar Muscular Atrophy, Spinal Muscular Atrophy Type 3, and Gastrostomy.

Stanley Sedore is a Pediatric Cardiologist practicing medicine in Traverse City, Michigan. He has been practicing medicine for over 16 years. Dr. Sedore is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Familial Dilated Cardiomyopathy, Brugada Syndrome, Short QT Syndrome, and Postural Orthostatic Tachycardia Syndrome (POTS). Dr. Sedore is board certified in American Board Of Pediatrics, Pediatric Cardiology - 2016 and American Board Of Pediatrics, Pediatrics - 2013.

Tomoyasu Higashimoto is a Medical Genetics specialist and an Internal Medicine provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. He is also highly rated in 110 other conditions, according to our data. His clinical expertise encompasses Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia. Dr. Higashimoto is board certified in Family Medicine and Clinical Genetics & Genomics.

Ann Little is a Neurologist and a Neuroradiologist practicing medicine in Ann Arbor, Michigan. Dr. Little is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 63 other conditions, according to our data. Her clinical expertise encompasses Inclusion Body Myositis, Polymyositis, Myasthenia Gravis, Stent Placement, and Transmyocardial Revascularization.

Cooking, spending time with my family. Dr. Ames is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Cardiomyopathic Lentiginosis, Cardiofaciocutaneous Syndrome, and Noonan Syndrome. Dr. Ames is board certified in Pediatrics, Clinical Genetics & Genomics, and Medical Biochemical Genetics.

Dr. Feldman is the director of the NeuroNetwork for Emerging Therapies at Michigan Medicine and the ALS Center of Excellence at Michigan Medicine. The latter includes the Pranger ALS Clinic, one of the top multidisciplinary clinics caring for those suffering from amyotrophic lateral sclerosis (ALS). She serves as the University of Michigan James W. Albers Distinguished University Professor and the Russell N. DeJong Professor of Neurology at Michigan Medicine. Dr. Feldman is one of the world’s leading authorities on neurodegenerative disease.Dr. Feldman is a compassionate and dedicated physician who cares deeply about her patients. She has been recognized for her clinical excellence by numerous organizations and is annually named as one of the “Best Doctors in America.” Her forward-thinking, collaborative, multidisciplinary approach has transformed how neurodegenerative diseases are diagnosed, treated, and prevented.Dr. Feldman has made significant contributions to biomedical research and clinical care in many critical areas of neurodegenerative disease. She has authored over 530 peer-reviewed publications, 74 book chapters, and 5 books on the pathology, diagnosis, and treatment of neurological diseases. Dr. Feldman has been continuously funded by the NIH since 1989 and is currently the principal or co-investigator of numerous clinical trials and grants. She has received numerous awards and honors throughout her remarkable career, including the University of Michigan’s Early Distinguished Career Award, the Distinguished Faculty Achievement Award, and the Distinguished Alumnus Achievement Award. She was also the first woman in 25 years to receive the Robert S. Schwab Award from the American Clinical Neurophysiology Society. In 2022, Dr. Feldman was awarded the University of Michigan Distinguished Professorship, the highest faculty honor at University of Michigan.Dr. Feldman is actively committed to and involved in professional service. She served as President of the Peripheral Nerve Society from 2007-2009 and President of the American Neurological Association (ANA) from 2011-2013. Dr. Feldman is an elected member of the National Academy of Medicine (NAM) and Association of American Physicians, and a Fellow of the American Association for the Advancement of Science. Dr. Feldman is the Editor of the Contemporary Neurology Series and also serves on a number of editorial boards for leading scientific journals, including The Lancet Neurology, Nature Reviews Neurology, JAMA Neurology and Journal of Neurology, Neurosurgery and Psychiatry. Dr. Feldman is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 33 other conditions, according to our data. Her clinical expertise encompasses Peripheral Neuropathy, Diabetic Neuropathy, Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease), and Autonomic Neuropathy. Dr. Feldman is board certified in Neurology and Electrodiagnostic Medicine.

Stacie Adams is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Grand Rapids, Michigan. Dr. Adams is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactose Epimerase Deficiency. Dr. Adams is currently accepting new patients.

William Murray is a primary care provider, practicing in Internal Medicine in Novi, Michigan. Dr. Murray is rated as an Experienced provider by MediFind in the treatment of Carnitine Palmitoyltransferase 1 Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Cluster Headache, Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, and Hypertension.