The 20 Best Tyrosinemia Type 1 Doctors Near Me

Willem Van Ginkel practices practicing medicine in Groningen, Netherlands. Van Ginkel is rated as an Elite expert by MediFind in the treatment of Tyrosinemia Type 1. They are also highly rated in 1 other condition, according to our data. Their clinical expertise encompasses Tyrosinemia Type 1, Phenylketonuria (PKU), Porphyria, and Vitamin B12 Deficiency Anemia.

Markus Grompe is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Portland, Oregon. Dr. Grompe is rated as an Elite provider by MediFind in the treatment of Tyrosinemia Type 1. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Congenital Aplastic Anemia, Tyrosinemia Type 1, Phenylketonuria (PKU), Islet Cell Transplantation, and Hepatectomy.

. Dr. Narumanchi is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 1. He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Narumanchi is board certified in American Board Of Medical Genetics And Genomics.

Margaretha Fokkema-Heiner practices practicing medicine in Groningen, Netherlands. Ms. Fokkema-Heiner is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1, Phenylketonuria (PKU), Medium-Chain Acyl-CoA Dehydrogenase Deficiency, Kidney Transplant, and Ileostomy.

Francjan Van Spronsen practices practicing medicine in Groningen, Netherlands. Van Spronsen is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. They are also highly rated in 7 other conditions, according to our data. Their clinical expertise encompasses Phenylketonuria (PKU), Tyrosinemia Type 1, Maternal Hyperphenylalaninemia, and Molybdenum Cofactor Deficiency (MoCD).

Francjan Van Spronsen-Spronsen practices practicing medicine in Groningen, Netherlands. Van Spronsen-Spronsen is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. They are also highly rated in 2 other conditions, according to our data. Their clinical expertise encompasses Phenylketonuria (PKU), Tyrosinemia Type 1, Maternal Hyperphenylalaninemia, and Molybdenum Cofactor Deficiency (MoCD).

Peter Baker is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Aurora, Colorado. Dr. Baker is rated as a Distinguished provider by MediFind in the treatment of Tyrosinemia Type 1. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Tyrosinemia Type 3, Tyrosinemia Type 1, Tyrosinemia Type 2, and Maple Syrup Urine Disease. Dr. Baker is currently accepting new patients.

Anita Macdonald practices practicing medicine in Birmingham, United Kingdom. Ms. Macdonald is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 13 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Tyrosinemia Type 1, Gastrostomy, and Liver Embolization.

Carolina Arias practices practicing medicine in Santiago, Chile. Ms. Arias is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1, Phenylketonuria (PKU), Maple Syrup Urine Disease, and Dihydrolipoamide Dehydrogenase Deficiency.

Philippe Goyens practices practicing medicine in Brussels, Belgium. Mr. Goyens is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Tyrosinemia Type 1, Hirschsprung Disease, Phenylketonuria (PKU), and Malnutrition.

Veronica Cornejo practices practicing medicine in Santiago, Chile. Ms. Cornejo is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1, Phenylketonuria (PKU), Dihydrolipoamide Dehydrogenase Deficiency, and Maple Syrup Urine Disease.

Marelle Bouva practices practicing medicine in Bilthoven, Netherlands. Ms. Bouva is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1, Classic Galactosemia, Neonatal Hypothyroidism, and Adrenoleukodystrophy (ALD).

Karen Fuenzalida practices practicing medicine in Santiago, Chile. Ms. Fuenzalida is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1 and Phenylketonuria (PKU).

Paula Waters practices practicing medicine in Sherbrooke, Canada. Ms. Waters is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 4 other conditions, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Malonyl-CoA Decarboxylase Deficiency, and Propionic Acidemia.

Genevieve Morrow practices practicing medicine in Quebec, Canada. Ms. Morrow is rated as a Distinguished expert by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Tyrosinemia Type 1.

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 Tyrosinemia Type 1. He is also highly rated in 177 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and Argininosuccinic Aciduria.

Laura Mackay is a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Mackay is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 132 other conditions, according to our data. Her clinical expertise encompasses Isovaleric Acidemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Adrenoleukodystrophy (ALD).

Amy Kritzer is a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Kritzer is rated as an Advanced provider by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 33 other conditions, according to our data. Her clinical expertise encompasses Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome). Dr. Kritzer is board certified in Pediatrics, Medical Biochemical Genetics, and Clinical Genetics And Genomics.

Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as an Experienced provider by MediFind in the treatment of Tyrosinemia Type 1. She is also highly rated in 28 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation. Dr. Hamosh is board certified in American Board Of Medical Genetics And Genomics.

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 Tyrosinemia Type 1. 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.