The 20 Best Homocystinuria Doctors Near Me in Maryland, US

Charles Venditti is a Medical Genetics provider practicing medicine in Bethesda, Maryland. Dr. Venditti is rated as an Elite provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Methylmalonic Acidemia, Propionic Acidemia, Homocystinuria, and Niemann-Pick Disease.

George Bone is a primary care provider, practicing in Internal Medicine in Upper Marlboro, Maryland. Dr. Bone is rated as a Distinguished provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 27 other conditions, according to our data. His clinical expertise encompasses Homocystinuria, Methylmalonic Acidemia with Homocystinuria, Vitamin D Deficiency, and Inborn Amino Acid Metabolism Disorder.

Hind Alsharhan is a Medical Genetics provider practicing medicine in Baltimore, Maryland. Dr. Alsharhan is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses ALG3-CDG, Ornithine Transcarbamylase Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, and Phenylketonuria (PKU). Dr. Alsharhan is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Shira Ziegler is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Ziegler is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Hypercementosis, Inborn Amino Acid Metabolism Disorder, Homocystinuria, and Maple Syrup Urine Disease. Dr. Ziegler is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Dr. Couser obtained his bachelor’s degree from the University of Virginia and his Medical Doctorate from the Virginia Commonwealth University School of Medicine (VCU SOM). Dr. Couser’s ophthalmology residency was completed at Howard University where he served as co-chief resident in the last year of his residency. He received fellowship training in pediatric ophthalmology and adult strabismus at Emory University. Dr. Couser received a master’s degree in biotechnology from the Johns Hopkins University and completed a residency in clinical genetics at the University of North Carolina at Chapel Hill. He is one of only a few individuals currently board-certified by both the American Board of Ophthalmology and the American Board of Medical Genetics and Genomics. CV https://www.hopkinsmedicine.org/-/media/wilmer/documents/cvs/couser-cv Research Summary My primary research focus involves the identification and management of genetic eye diseases including rare inherited disorders affecting the eyes. Research and scholarly activities have been an integral component of my career path. I have been the principal investigator on 10 clinical trial/IRB studies and a co-investigator on others, participated with several committees or advisory panels related to research activities. I have been credited with over 120 book chapter, journal article and abstract publications. In addition, I served as the primary author/sole editor for a textbook titled Ophthalmic Genetic Diseases: A Quick Reference Guide to the Eye and External Ocular Adnexa Abnormalities, 1st Edition, published by Elsevier in 2018, which is one of only a few textbooks published in this subject area. I also served as a grant review panelist for the National Eye Institute Career Development Awards. Selected Publications *Couser NL, Masood MM, Strande NT, Foreman AKM, Crooks K, Weck KE, Lu M, Wilhelmsen KC, Roche M, Evans JP, Berg JS, Powell CM. 2015. The phenotype of multiple congenital anomalies- hypotonia-seizures syndrome 1: Report and review. Am J Med Genet Part A 9999A:1–6 *Couser NL, Lambert SR. Botulinum toxin: A treatment of consecutive esotropia in children. Strabismus 2012; 20(4):158-161 Couser NL, Lenhart PD, Hutchinson AK. Augmented Hummelsheim procedure to treat complete abducens nerve palsy. J AAPOS 2012;16(4):331-5 *Natario L. Couser, Maheer M. Masood, Arthur S. Aylsworth, and Roger E. Stevenson. Ocular manifestations in the X-linked intellectual disability syndromes. Ophthalmic Genet. 2017, Jan 23:1-12 *Couser NL, Brooks BP, Drack AV, Shankar SP. The evolving role of genetics in ophthalmology. Ophthalmic Genet. 2021 Jan 12:1-4. doi: 10.1080/13816810.2020.1868011. Dr. Couser is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Epicanthal Folds, Strabismus, Hypotonia, and Brown Syndrome. Dr. Couser is board certified in American Board Of Medical Genetics And Genomics and American Board Of Ophthalmology.

Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, and Progressive External Ophthalmoplegia. Dr. Vernon is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Riaz Janjua, MD, specializes in neurology and is board certified in neurology by the American Board of Psychiatry and Neurology. He practices at UPMC Western MD Specialty Services - Neurology. Dr. Janjua completed his residency at St Vincent Hospital of New York and medical education at King Edward Medical College. Dr. Janjua is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 28 other conditions, according to our data. His clinical expertise encompasses Memory Loss, Dravet Syndrome, Progressive Myoclonic Epilepsy, and Epilepsy. Dr. Janjua is board certified in American Board Of Psychiatry And Neurology. Dr. Janjua is currently accepting new patients.

"Dr. Ari D. Fishman is a hematologist affiliated with Sibley Memorial Hospital, Holy Cross Hospital and George Washington University Hospital, where he serves as an assistant professor of medicine for the School of Medicine. He practices out of Maryland Oncology and Hematology, located in Wheaton, Maryland and Silver Spring, Maryland. Dr. Fishman earned his medical degree from Sackler School of Medicine. He completed a residency in internal medicine at the Beth Israel Medical Center, followed by a fellowship in hematology and oncology at the Montefiore Medical Center. Dr. Fishman previously worked at Washington Oncology Hematology Center, located in Washington, D.C. and Chevy Chase, Maryland. Dr. Fishman has been named a Top Doctor in Hematology and Oncology by Washingtonian Magazine and a Top Doctor by Consumers’ Checkbook magazine. Dr. Fishman is a member of the American College of Physicians and the American Society of Clinical Oncology. Dr. Fishman has contributed to numerous publications. Selected Publications Fishman AD, Hoffman A, Volterra F, Frymus M, Gentilluci M. ""Intracaval and intracardiac metastatic nonseminomatous germ cell tumor: a rare cause of hemolytic anemia and thrombocytopenia."" Cancer Invest. 2002;20(7-8):996-1001.". Dr. Fishman is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 55 other conditions, according to our data. His clinical expertise encompasses Monoclonal Gammopathy of Undetermined Significance (MGUS), Schnitzler Syndrome, Myelodysplastic Syndrome (MDS), and Childhood Iron Deficiency Anemia. Dr. Fishman is board certified in American Board Of Internal Medicine.

Husna Baksh is a primary care provider, practicing in Internal Medicine in Silver Spring, Maryland. Dr. Baksh is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. She is also highly rated in 18 other conditions, according to our data. Her clinical expertise encompasses Hypertensive Heart Disease, Vitamin D Deficiency, Enlarged Liver, and Pediatric Myocarditis.

Deepnarayan Tiwarri is an Oncologist practicing medicine in Brandywine, Maryland. Dr. Tiwarri is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 85 other conditions, according to our data. His clinical expertise encompasses Childhood Iron Deficiency Anemia, Iron Deficiency Anemia, Pulmonary Embolism, and Anemia.

Mohammad Meelu is a Hematologist practicing medicine in Waldorf, Maryland. Dr. Meelu is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 14 other conditions, according to our data. His clinical expertise encompasses Blood Clots, Vitamin B12 Deficiency, Pleuropulmonary Blastoma, and Subacute Combined Degeneration.

Gregory Pokrywka is a primary care provider, practicing in Internal Medicine in Towson, Maryland. Dr. Pokrywka is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 17 other conditions, according to our data. His clinical expertise encompasses Abdominal Obesity Metabolic Syndrome, Type B Insulin Resistance Syndrome, Cytochrome C Oxidase Deficiency, and Mitochondrial Complex V Deficiency. Dr. Pokrywka is currently accepting new patients.

Kelson Figaro is a primary care provider, practicing in Internal Medicine in Glenn Dale,, Maryland. Dr. Figaro is rated as an Advanced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Vitamin D Deficiency, Obesity, Homocystinuria, Methylmalonic Acidemia with Homocystinuria, and Gastrostomy.

Ayesha Butt, M.D., practices internal medicine at Johns Hopkins Community Physicians Water's Edge. She received her medical degree from Dow Medical College Dow University of Health Sciences, and also completed her residency at Brookdale Hospital Medical Center. Dr. Butt is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Peripheral Artery Disease, Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, and Familial Hypertension. Dr. Butt is board certified in American Board Of Internal Medicine.

Swati D Phatak, M.D., practices internal medicine at Johns Hopkins Community Physicians Greater Dundalk. She received her medical degree from Topiwala National Medical College in Mumbai, India. Dr. Phatak completed residencies at Grant Medical College University of Mumbai and at State University of New York Upstate Medical University in Syracuse, New York. She speaks English, Hindi and Marathi. Dr. Phatak is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Vitamin D Deficiency, Hypertension, Glucocorticoid-Remediable Aldosteronism, and Familial Hypertension. Dr. Phatak is board certified in American Board Of Internal Medicine.

Amar Duggirala is a primary care provider, practicing in Family Medicine in Poolesville, Maryland. Dr. Duggirala is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Sitosterolemia, Bronchitis, High Cholesterol, and Pheochromocytoma.

Jose Mendoza is an Oncologist practicing medicine in Clinton, Maryland. Dr. Mendoza is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 68 other conditions, according to our data. His clinical expertise encompasses Childhood Iron Deficiency Anemia, Iron Deficiency Anemia, Anemia, and Familial Colorectal Cancer.

Russell De Luca is a Hematologist practicing medicine in Annapolis, Maryland. Dr. De Luca is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Pleuropulmonary Blastoma, Paget Disease of the Breast, Breast Cancer, and Lung Cancer.

Rita Gupta is an Oncologist practicing medicine in Brandywine, Maryland. Dr. Gupta is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. She is also highly rated in 50 other conditions, according to our data. Her clinical expertise encompasses Iron Deficiency Anemia, Childhood Iron Deficiency Anemia, Paget Disease of the Breast, and Breast Cancer.

William Queale is a primary care provider, practicing in Internal Medicine in Lutherville Timonium, Maryland. Dr. Queale is rated as an Experienced provider by MediFind in the treatment of Homocystinuria. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Methylmalonyl Coenzyme A Mutase Deficiency, Methylmalonic Acidemia, Methylmalonic Acidemia with Homocystinuria, and Homocystinuria.