The 20 Best Inborn Amino Acid Metabolism Disorder Doctors Near Me in Bronx, NY

Rajesh Bhatnagar is a Neurologist practicing medicine in Bronx, New York. Dr. Bhatnagar is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 25 other conditions, according to our data. His clinical expertise encompasses Andermann Syndrome, Sensorimotor Polyneuropathy, Hereditary Sensory Neuropathy Type 1 (HSN1), and Septic Arthritis.

Rashid Ahmed is a primary care provider, practicing in Family Medicine in Bronx, New York. Dr. Ahmed is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Obesity, Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Gastric Bypass, and Sleeve Gastrectomy.

Sandeep Malik is an Internal Medicine provider practicing medicine in Bronx, New York. Dr. Malik is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 34 other conditions, according to our data. His clinical expertise encompasses Malabsorption, Deep Vein Thrombosis, Essential Thrombocythemia, and Intraductal Papilloma.

Natalya Rodionova is a primary care provider, practicing in Family Medicine in Bronx, New York. Dr. Rodionova is rated as an Advanced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Anemia, Scurvy, Urea Cycle Disorders (UCD), and Arginase Deficiency.

Alejandro Iglesias, MD is Assistant Professor of Pediatrics, Director of the Inherited Metabolic Program, Program Director of the Medical Genetics Residency program and Attending Physician in the Division of Medical Genetics, Department of Pediatrics at New York Presbyterian Hospital/Columbia University Medical Center. He is a clinical and biochemical geneticist primarily interested in inherited metabolic disorders and neurogenetics and dysmorphology. In his role as Director of the Inherited Metabolic Program he is deeply involved in all aspects related with the diagnosis, management and overall care of patients and families with these disorders. In addition, he is in charge of the education of young physicians and medical students in the field of IMD. As an educator, he is in charge of the medical biochemistry lecture series for the first year medical students at the Physicians & Surgeons Medical School at Columbia University paving the way for a new generations of brilliant medical students at Columbia University. Finally, his involvement with the diagnosis and care of patients with X-linked adrenoleukodystrophy has been one of his main accomplishments in the recent years, especially since the introduction of newborn screening in New York State. He has a been involved from the beginning in the development of the program and is active member of the NYS group of metabolic physicians taking care of these patients. In addtion he has been actively involved in all developments asscoiated with newborn screening for Krabbe disease and Pompe disease. Dr. Iglesias is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Hypotonia, Microcephaly, Achalasia Microcephaly Syndrome, and Cortical Dysplasia. Dr. Iglesias is board certified in Pediatrics, Clinical Genetics And Genomics (MD), and Clinical Biochemical Genetics. Dr. Iglesias is currently accepting new patients.

Alain Sosa is a primary care provider, practicing in Internal Medicine in Elmhurst, New York. Dr. Sosa is rated as a Distinguished provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 51 other conditions, according to our data. His clinical expertise encompasses Methylmalonic Acidemia with Homocystinuria, Homocystinuria, Inborn Amino Acid Metabolism Disorder, and High Cholesterol.

Dr. Ian Daniel Krantz, MD, is a renowned physician specializing in Genetics and Pediatrics. He currently sees patients at Cohen Children's Medical Center (CCMC) and Northwell Health Physician Partners Medical Genetics. Dr. Krantz holds certifications in Clinical Genetics, Cytogenetics, and Pediatrics from the American Board of Medical Genetics and the American Board of Pediatrics, respectively.Dr. Krantz completed his BFA at Concordia University in Montreal and his MD at Sackler School of Medicine (Tel Aviv University). He completed his residency in Medical Genetics at Children's Hospital of Philadelphia and his residency in Pediatrics at New York University Medical Center.With an impressive set of academic and administrative titles, Dr. Krantz serves as the Division Chief of Pediatric Genetics and Genomics at Cohen Children's Medical Center and is the System Vice President for Pediatric Genetics at Northwell Health. Additionally, he holds the position of Professor at the Zucker School of Medicine at Northwell Health.Dr. Krantz is recognized for his clinical expertise in isolated and syndromic forms of congenital birth differences and developmental diagnoses, including syndromic and non-syndromic autism. He has a special interest in the genetics of hearing loss and focused expertise in Cornelia de Lange Syndrome, Pallister-Killian syndrome, Alagille syndrome, CHOPS syndrome, among others.Dr. Krantz's research is dedicated to identifying and characterizing the molecular etiology of syndromic and non-syndromic developmental diagnoses. His research lab has made significant contributions in the field, discovering new disease genes and shedding light on critical molecular pathways involved in human developmental disorders.Driven by his commitment to advancing patient care, Dr. Krantz has been at the forefront of integrating genomic technologies into the clinical setting. He has implemented rapid genome sequencing into the NICU and CICU and established biobanks and biorepositories to further research efforts. Through his work, he aims to understand the impact of complex diagnostic information on clinicians and families involved.With his extensive expertise and dedication to advancing genetic research and patient care, Dr. Krantz continues to make significant contributions to the field of Pediatrics and Genetics. Dr. Krantz is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 15 other conditions, according to our data. His clinical expertise encompasses Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.

Shahanaz Begum is a primary care provider, practicing in Family Medicine in Bronx, New York. Dr. Begum is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. Her clinical expertise encompasses Primary Hyperoxaluria, Vitamin D Deficiency, High Cholesterol, and Gastroesophageal Reflux Disease (GERD).

Warren Geisler is a primary care provider, practicing in Internal Medicine in Bronx, New York. Dr. Geisler is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Vitamin B12 Deficiency, Subacute Combined Degeneration, Maturity Onset Diabetes of the Young, and Tracheitis.

Anas Mogharbel is a Hematologist and an Oncologist practicing medicine in Bronx, New York. Dr. Mogharbel is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Thalassemia, Anemia, Childhood Iron Deficiency Anemia, and Iron Deficiency Anemia.

Yomaris Pena is a primary care provider, practicing in Internal Medicine in New York, New York. Dr. Pena is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Obesity in Children, Transcobalamin Deficiency, Sitosterolemia, and Food Allergy.

Alvin Lindsay is a primary care provider, practicing in Internal Medicine in New York, New York. Dr. Lindsay is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Sciatica, Scoliosis, Folate Deficiency, and Vitamin B12 Deficiency Anemia.

Sonam Verma is a Neurologist practicing medicine in New York, New York. Dr. Verma is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Seizures, Generalized Tonic-Clonic Seizure, Landau-Kleffner Syndrome, and Memory Loss.

Ralph Essien is a primary care provider, practicing in Internal Medicine in New Rochelle, New York. Dr. Essien is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Peripheral Artery Disease, Obesity, Bronchitis, and Coronary Heart Disease.

Helio Pedro is a Pediatrics provider practicing medicine in Hackensack, New Jersey. Dr. Pedro is rated as an Experienced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Glycine Encephalopathy, Biotinidase Deficiency, Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia. Dr. Pedro is board certified in American Board Of Medical Genetics And Genomics.

Jiansheng Zhao is a primary care provider, practicing in Internal Medicine in Flushing, New York. He has been practicing medicine for over 44 years. Dr. Zhao is rated as an Advanced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 57 other conditions, according to our data. His clinical expertise encompasses Sitosterolemia, High Cholesterol, Muscle Spasms, and Opisthotonos.

George Diaz is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Diaz is rated as an Advanced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Argininosuccinic Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Urea Cycle Disorders (UCD), and Ornithine Transcarbamylase Deficiency.

Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Breilyn is rated as an Advanced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. She is also highly rated in 42 other conditions, according to our data. Her clinical expertise encompasses Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Phenylketonuria (PKU).

Jaya Ganesh is a Pediatrics provider practicing medicine in New York, New York. Dr. Ganesh is rated as an Advanced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. She is also highly rated in 64 other conditions, according to our data. Her clinical expertise encompasses Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Danon Disease.

Mary Lopiccolo is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Lopiccolo is rated as an Advanced provider by MediFind in the treatment of Inborn Amino Acid Metabolism Disorder. She is also highly rated in 30 other conditions, according to our data. Her clinical expertise encompasses Glutaric Acidemia Type 2, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Carnitine Palmitoyltransferase 1 Deficiency.