The 20 Best PEPCK 1 Deficiency Doctors near New York, NY

Philip Paty is a Colorectal Surgeon in New York, New York. Dr. Paty is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Colorectal Cancer, Anal Cancer, Lynch Syndrome, Colostomy, and Ileostomy.

Leonard Saltz is an Oncologist in New York, New York. Dr. Saltz is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Colorectal Cancer, Lynch Syndrome, Familial Colorectal Cancer, Liver Embolization, and Tissue Biopsy. Dr. Saltz is currently accepting new patients.

Yelena Janjigian is an Oncologist in New York, New York. Dr. Janjigian is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Gastroesophageal Junction Cancer, Stomach Cancer, Esophageal Cancer, Liver Embolization, and Endoscopy. Dr. Janjigian is currently accepting new patients.

Sohail Tavazoie is an Oncologist in New York, New York. Dr. Tavazoie is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are PEPCK 1 Deficiency, Breast Cancer, Colorectal Cancer, and Liver Cancer.

Sheemon Zackai is a Pediatrics provider in New York, New York. Dr. Zackai is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Multisystem Inflammatory Syndrome in Children (MIS-C), Dihydrolipoamide Dehydrogenase Deficiency, Pyruvate Carboxylase Deficiency, and Autosomal Recessive Congenital Methemoglobinemia.

Jaya Ganesh is a Pediatrics provider in New York, New York. Dr. Ganesh is rated as an Advanced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Danon Disease.

Ibrahim Elsharkawi is a Pediatrics provider in New York, New York. Dr. Elsharkawi is rated as an Advanced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are MELAS Syndrome, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Tyrosinemia Type 3.

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 PEPCK 1 Deficiency. His top areas of expertise are Hypotonia, Microcephaly, Achalasia Microcephaly Syndrome, and Cortical Dysplasia.

Jennifer Bain, MD, PhD, is an Associate Professor of Neurology and Pediatrics at the Columbia University Medical Center. Dr. Bain completed both an MD and PhD, as well as general pediatrics residency at Rutgers – New Jersey Medical School in New Jersey. She then trained in Child Neurology at NewYork-Presbyterian/Columbia University Irving Medical Center in New York City and is a board-certified neurologist with special certification in Child Neurology seeing both inpatient and outpatient pediatric neurology patients. Her clinic focuses on diagnosis and management of autism, cerebral palsy and neurodevelopmental disorders in addition to genetic disorders associated with such conditions.Her early research career focused on spinal cord and brain development after injuries such as spinal cord injury and perinatal hypoxic ischemic encephalopathy. During her residency training, her clinical research focused on studying autonomic dysfunction in children with autism spectrum disorders and neurological complications during extracorporeal membrane oxygenation. She currently works as a physician scientist at Columbia University specializing in general pediatric neurology with expertise in development, behavioral neurology, autism and cerebral palsy. Her clinical research has focused on studying the genetics of neurodevelopmental disorders including autism and cerebral palsy. The genes she has worked closely on include HNRNPH2 and related disorders, GRIN disorders, KIF1A. She is interested in understanding clinically meaningful measures in families affected by neurodevelopmental disorders and measuring longitudinal trajectories in such disorders. She has been working closely with several patient advocacy groups, researchers, and Simons Searchlight to continuously move forward in the understanding of the developing and aging brain. Dr. Bain is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are HNRNPH2-Related Disorder, Autism Spectrum Disorder, Early Infantile Epileptic Encephalopathy, and Cerebral Palsy.

Rachel Brozinsky is a Pediatrics provider in Astoria, New York. Dr. Brozinsky is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Multiple Pterygium Syndrome X Linked, Amniotic Band Syndrome, Multiple Pterygium Syndrome, and Popliteal Pterygium Syndrome.

Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Breilyn is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Phenylketonuria (PKU).

Emily Hertzberg is a Pediatrics provider in New York, New York. Dr. Hertzberg is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Infant Botulism, PEPCK 1 Deficiency, Autosomal Recessive Congenital Methemoglobinemia, Pyruvate Carboxylase Deficiency, and Adenoidectomy.

Kimihiko Oishi is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Oishi is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Micrognathia, Citrullinemia, Urea Cycle Disorders (UCD), and Methylmalonic Acidemia with Homocystinuria.

Meyer Kattan is a Pediatrics provider in New York, New York. Dr. Kattan is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Asthma, Asthma in Children, Stridor, and Anemia. Dr. Kattan is currently accepting new patients.

Helio Pedro is a Pediatrics provider in Hackensack, New Jersey. Dr. Pedro is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Glycine Encephalopathy, Biotinidase Deficiency, Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia.

John Rausch is an Internal Medicine provider in New York, New York. Dr. Rausch is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Obesity in Children, Autosomal Recessive Congenital Methemoglobinemia, Pyruvate Carboxylase Deficiency, and Dihydrolipoamide Dehydrogenase Deficiency.