The 20 Best Andersen Disease Doctors in The United States

Kumaraswamy Sivakumar is a Neurologist practicing medicine in Phoenix, Arizona. Dr. Sivakumar is rated as a Distinguished provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 73 other conditions, according to our data. His clinical expertise encompasses Inclusion Body Myositis, Myasthenia Gravis, Chronic Inflammatory Demyelinating Polyneuropathy, and Dermatomyositis. Dr. Sivakumar is board certified in Psychiatry & Neurology (Neurology), Psychiatry & Neurology (Sub: Clinical Neurophysiolog, and Psychiatry & Neurology (Sub: Neuromuscular Medicine). Dr. Sivakumar is currently accepting new patients.

Jennifer Murphy is a Neurologist practicing medicine in Philadelphia, Pennsylvania. Dr. Murphy is rated as a Distinguished provider by MediFind in the treatment of Andersen Disease. She is also highly rated in 26 other conditions, according to our data. Her clinical expertise encompasses Andersen Disease, Adult Polyglucosan Body Disease, CACH Syndrome, and Pelizaeus-Merzbacher Disease. Dr. Murphy is board certified in Neurology, 2014. Dr. Murphy is currently accepting new patients.

Charulatha Nagar is a Neurologist practicing medicine in Glenview, Illinois. She has been practicing medicine for over 36 years. Dr. Nagar is rated as a Distinguished provider by MediFind in the treatment of Andersen Disease. She is also highly rated in 18 other conditions, according to our data. Her clinical expertise encompasses Glycogen Storage Disease Type 13, Adult Polyglucosan Body Disease, Andersen Disease, and Glycogen Storage Disease Type 9. Dr. Nagar is board certified in American Board Of Psychiatry And Neurology - Neurology (Certified).

Mari Mori is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Orlando, Florida. Dr. Mori is rated as an Advanced provider by MediFind in the treatment of Andersen Disease. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses FG Syndrome, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Von Gierke Disease, and Ornithine Transcarbamylase Deficiency. Dr. Mori is currently accepting new patients.

Laurie Seaver is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Grand Rapids, Michigan. Dr. Seaver is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Hypotonia, 1p36 Deletion Syndrome, Smith-Magenis Syndrome, and Potocki-Lupski Syndrome. Dr. Seaver is currently accepting new patients.

Claudia Soler-Alfonso is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Houston, Texas. Dr. Soler-Alfonso is rated as a Distinguished provider by MediFind in the treatment of Andersen Disease. She is also highly rated in 13 other conditions, according to our data. Her clinical expertise encompasses Andersen Disease, Leigh Syndrome, Potocki-Lupski Syndrome, and Von Gierke Disease. Dr. Soler-Alfonso is currently accepting new patients.

Luis Umana is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 177 other conditions, according to our data. His clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Classic Galactosemia, Biotinidase Deficiency, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.

Jose Abdenur is a Medical Genetics provider practicing medicine in Orange, California. Dr. Abdenur is rated as an Advanced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses Glycogen Storage Disease Type 9, Von Gierke Disease, Glycogen Storage Disease Type 3, and Malonyl-CoA Decarboxylase Deficiency. Dr. Abdenur is currently accepting new patients.

Richard Chang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chang is rated as an Advanced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 155 other conditions, according to our data. His clinical expertise encompasses Citrullinemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Adrenoleukodystrophy (ALD). Dr. Chang is currently accepting new patients.

Sumit Parikh is a Pediatric Neurologist practicing medicine in Cleveland, Ohio. He has been practicing medicine for over 32 years. Dr. Parikh is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 168 other conditions, according to our data. His clinical expertise encompasses Leigh Syndrome, Maternally Inherited Leigh Syndrome, Kearns-Sayre Syndrome, and MELAS Syndrome. Dr. Parikh is board certified in American Board Of Psychiatry And Neurology, 2006.

David Rodriguez is a Pediatrics provider practicing medicine in Houston, Texas. He has been practicing medicine for over 27 years. Dr. Rodriguez is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Achondroplasia, Von Gierke Disease, Acanthosis Nigricans, Adenoidectomy, and Myringotomy.

Marvin Natowicz is a Medical Genetics provider practicing medicine in Cleveland, Ohio. He has been practicing medicine for over 50 years. Dr. Natowicz is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Autism Spectrum Disorder, Fragile X Syndrome, Andersen Disease, and Cardiomyopathic Lentiginosis. Dr. Natowicz is board certified in American Board Of Medical Genetics And Genomics, 1990.

I find joy and satisfaction in my dedication to the care of children with rare diseases specifically: genetic disorders and inherited disorders of metabolism. Due to many years of training and practice, I have experience involving care of patients with a variety of genetic and metabolic conditions, including but not limited to glycogen storage diseases, fatty acid oxidation defects, mitochondrial disorders, lysosomal storage diseases, urea cycle disorders, organic acidurias, aminoacidopathies, and infantile hepatopathy due to LARS mutations, etc. I enjoy working together with children and their parents, whom I consider an important part of the team. I pursued this field because it gives me great satisfaction and pleasure to see the children with these conditions grow, and the patients and families feel cared for, and not isolated. I love learning about the children's interests, and see that they grow happy and healthy. I think out of the box when there is a challenge that needs to be met for the patient's care and management. Dr. Hassan is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Mitochondrial Trifunctional Protein Deficiency, Protein Deficiency, Von Gierke Disease, and Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. Dr. Hassan is board certified in American Board Of Medical Genetics And Genomics, Clinical Genetics and American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics.

Dr. Schiffmann is a renowned expert on neurometabolic diseases. He earned his medical degree from the University of Liège, Belgium and a Master of Health Sciences in Clinical Research from Duke University. He is board-certified in Neurology with a Special Qualification in Child Neurology and is a Fellow of the American Academy of Neurology. Dr. Schiffmann was a lead researcher at the United States National Institutes of Health in Bethesda, Maryland for over 17 years (1991-2007) and then the Director of the Institute of Metabolic Disease at the Baylor Scott & White Research Institute in Dallas, Texas, 2008-2019. Dr. Schiffmann is a Professor in the Department of Internal Medicine, Texas Christian University and a Clinical Professor, Texas A&M University Medical School College of Medicine. He is also a Senior Vice President for Clinical Research at 4D Molecular Therapeutics. Dr. Schiffmann has been performing pre-clinical and clinical research on lysosomal storage diseases since 1991 with a special focus on the natural history, pathogenesis and therapy of Fabry disease, Gaucher disease and the leukodystrophies. One of his particular interests and areas of expertise is to address patients with undiagnosed neurological diseases. Dr. Schiffmann has published 276 peer-reviewed research articles and over 15 book chapters. Dr. Schiffmann is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Gaucher Disease Type 3, Fabry Disease, Gaucher Disease, and Leukodystrophy. Dr. Schiffmann is board certified in Neurology With Special Qualification In Child Neurology- American Board Of Psychiatry And Neurology/Neurology With Special Qualification In Child Neurology and Neurology With Special Qualification In Child Neurology- American Board Of Psychiatry And Neurology.

Peter Kang is a Neuromusculoskeletal Medicine specialist and a Neurologist practicing medicine in Minneapolis, Minnesota. Dr. Kang is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Cockayne Syndrome, Limb-Girdle Muscular Dystrophy, Cockayne Syndrome Type 1, Cockayne Syndrome Type 2, and Thymectomy. Dr. Kang is board certified in Neuromuscular Medicine: American Board Of Psychiatry And Neurology, 2008, Clinical Neurophysiology: American Board Of Psychiatry And Neurology, 2003, and Pediatrics: American Board Of Pediatrics, 2001. Dr. Kang is currently accepting new patients.

Jonathan Zurawski is a Neurologist practicing medicine in Boston, Massachusetts. Dr. Zurawski is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Multiple Sclerosis (MS), Relapsing Multiple Sclerosis (RMS), Gerstmann Syndrome, and Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease. Dr. Zurawski is board certified in Neurology.

Dr. Changrui Xiao is a board-certified UCI Health neurologist, clinical geneticist and medical biochemical geneticist who specializes in neurogenetic and inherited metabolic disorders.His clinical interests include lysosomal storage diseases, hereditary and spinocerebellar ataxia, neurometabolic disorders, inborn errors of metabolism in adults, late onset Tay-Sachs and Sandhoff diseases, and genomic diagnosis.Xiao earned his medical degree at Duke University School of Medicine in Durham, N.C. He completed an internship in internal medicine and a residency in neurology at the University of Chicago Medical Center in Illinois. He received fellowship training in medical genetics and medical biochemical genetics at the National Institutes of Health Clinical Center and Johns Hopkins Hospital in Bethesda, Md., and Children's National Hospital in Washington, D.C. Before joining UCI Health, he was a clinician with the National Institutes of Health Undiagnosed Disease Program.He is the author or co-author of numerous peer-reviewed publications and presentations. He is an associate editor of the journalMolecular Genetics & Genomic Medicineand a consulting editor forGeneReviews. His goal is to provide a medical home for adults with neurogenetic and metabolic conditions, and to increase access to precision therapy for these conditions. Dr. Xiao is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Retinopathy Pigmentary Mental Retardation, Glutaric Acidemia Type 2, Adrenoleukodystrophy (ALD), and X-Linked Creatine Deficiency. Dr. Xiao is board certified in American Board Of Medical Genetics And Genomics - Clinical Genetics And Genomics and American Board Of Psychiatry And Neurology - Neurology.

Dr. Justin McArthur is nationally and internationally recognized for his work in studying the natural history, development and treatment of the neurological complications of HIV/AIDS, multiple sclerosis and other neurological infections and immune-mediated neurological disorders. Dr. McArthur has also developed a technique to use cutaneous nerves to study sensory neuropathies, including those associated with chemotherapy, HIV and diabetes. Currently his clinical practice includes neuroimmunological disorders including MS, neurological infections, and complex undiagnosed neurological disorders. Dr. McArthur was the founding director of the Johns Hopkins/National Institute of Mental Health Research Center for HIV-associated Cognitive Disorders. The Center is an experienced interdisciplinary research team who have pooled their talents to study the nature of HIV-associated cognitive disorders. he is also the founding director of the Johns Hopkins Sheikh Khalifa Stroke institute. Dr. McArthur received his medical degree from Guys Hospital Medical School in London, UK. He then completed an internship and residency in internal medicine at The Johns Hopkins Hospital in Baltimore, MD. Dr. McArthur stayed with Johns Hopkins to complete a residency in neurology and achieve his Master's in public health. He is the current Director of the Johns Hopkins Department of Neurology and holds the John W. Griffin Professorship in neurology which was established in 2015 by Jeffrey and Harriet Legum. In April 2017 Dr. McArthur was elected to the Association of American Physicians. In 2020 he was inducted into the National Academy of Medicine. Dr. Mcarthur is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Multiple Sclerosis (MS), Relapsing Multiple Sclerosis (RMS), Progressive Multifocal Leukoencephalopathy, and Encephalitis. Dr. Mcarthur is board certified in American Board Of Psychiatry And Neurology and American Board Of Internal Medicine.

Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New Hyde Park, New York. Dr. Fernandes is rated as an Experienced provider by MediFind in the treatment of Andersen Disease. She is also highly rated in 153 other conditions, according to our data. Her clinical expertise encompasses Microcephaly, Chromosome 13q Deletion, Hemihyperplasia, and Alstrom Syndrome.

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 Andersen Disease. 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.