The 20 Best Atelosteogenesis Type 1 Doctors Near Me in Maryland, US

Dr. Barañano earned her M.D. and Ph.D. degrees from the Johns Hopkins University School of Medicine, where she also completed residencies in pediatrics and neurology, along with a fellowship in neurogenetics at the Kennedy Krieger Institute. Dr. Barañano is an Associate Professor of Clinical Neurology. She specializes in the diagnosis and management of rare neurogenetic disorders. She has a particular interest in the genetic control and function of the cerebellum and expertise in childhood-onset and inherited ataxias. She is a member of the multidisciplinary Fetal Management group and is available for prenatal consultations. Dr. Barañano's research includes collaborative efforts with the Johns Hopkins Department of Genetic Medicine and the Division of Neurogenetics at the Kennedy Krieger Institute. Dr. Baranano is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. She is also highly rated in 22 other conditions, according to our data. Her clinical expertise encompasses Hypotonia, Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Focal or Multifocal Malformations in Neuronal Migration, and Spinocerebellar Ataxia Type 3. Dr. Baranano is board certified in American Board Of Psychiatry And Neurology.

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 Atelosteogenesis Type 1. 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. Grant Anhalt is a professor of dermatology at the Johns Hopkins University School of Medicine. His areas of clinical expertise include autoimmune skin diseases and dermatoimmunology. Dr. Anhalt serves as the director of the Dermatoimmunology Laboratory at the Johns Hopkins School of Medicine. He received his undergraduate degree and his M.D. from the University of Manitoba. He completed a residency in internal medicine at the Health Sciences Center in Winnipeg, Canada and a residency in dermatology at the University of Michigan. He performed a fellowship in immunodermatology at the University of Michigan Medical Center. Dr. Anhalt joined the Johns Hopkins faculty in 1982. He was interim chair of the Department of Dermatology from 1996 to 2001. His research interests include autoimmunity, bullous skin diseases and pemphigus and pemphigoid. Dr. Anhalt serves on the medical advisory board for the International Pemphigus & Pemphigoid Foundation. He has been recognized as a top doctor in the Washington Post Magazine, Baltimore Magazine and Castle Connolly Guide. He is a member of several professional organizations, including the American Academy of Dermatology, American Dermatologic Association and American Society for Clinical Investigation. CV http://www.hopkinsmedicine.org/dermatology/our_experts/CV/Anhalt_CV_2014.docx. Dr. Anhalt is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 24 other conditions, according to our data. His clinical expertise encompasses Pemphigus Vulgaris, Pemphigus, Bullous Pemphigoid, and Pemphigus Foliaceus. Dr. Anhalt is board certified in American Board Of Dermatology.

I am a pediatric neurologist with expertise in epilepsy and electroencephalography (EEG). My clinical and research interests include genetics of epilepsy, medical management of patients with intractable epilepsy and presurgical evaluation of patients who are candidates for epilepsy surgery. Dr. Gupta is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 9 other conditions, according to our data. His clinical expertise encompasses Seizures, Benign Rolandic Epilepsy, Rett Syndrome, Lennox-Gastaut Syndrome (LGS), and Thrombectomy. Dr. Gupta is board certified in American Board Of Psychiatry And Neurology.

Dr. Elrick specializes in the care of children with neuromuscular disorders, and EMG studies in children and adults. He has special interests in genetic neuromuscular and neurodegenerative disorders and Acute Flaccid Myelitis. Dr. Elrick earned his M.D. and Ph.D. in Neuroscience at the University of Michigan Medical School, studying inherited neurodegenerative disorders of childhood. He completed residency training in Pediatrics and Child Neurology, followed by a fellowship in Neuromuscular Medicine and Johns Hopkins before joining the faculty in 2019. Dr. Elrick's laboratory research interest is in understanding mechanisms of neurodegenerative disease, especially those affecting motor neurons. He studies disorders caused by genetic mutations in the nuclear pore complex, the main pathway for transport of material in and out of the nucleus of the cell, including Triple A Syndrome. He also participates in clinical research on Acute Flaccid Myelitis (AFM), aimed at understanding susceptibility to AFM in children, and defining clinical and EMG characteristics of illness and recovery in AFM. Dr. Elrick is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Cramp-Fasciculation Syndrome, Acute Flaccid Myelitis (AFM), Dysferlinopathy, and Duchenne Muscular Dystrophy. Dr. Elrick is board certified in American Board Of Psychiatry And Neurology.

Dr. Comi graduated from SUNY Buffalo School of Medicine and received her training in pediatrics at the Children's Hospital of Buffalo and her child neurology training at Johns Hopkins Medicine. Her clinical specialization is in the treatment of the neurological aspects of Sturge-Weber syndrome and other disorders related to capillary malformation. Dr. Comi's clinical research interests focus on improving the early diagnosis and treatment of brain involvement in Sturge-Weber syndrome in order to prevent ischemic brain injury in affected infants and young children, and on studies to understand what causes Sturge-Weber syndrome. Her laboratory research work deals with the pathogenesis of Sturge-Weber syndrome, recently shown to be caused by a somatic mutation, and on developing new drug targets, screening assays, models and therapeutic strategies for Sturge-Weber syndrome. Her lab group also works on developing better neuroprotective and neuroregenerative responses to brain injury resulting from impaired blood flow to the brain. Dr. Comi is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. She is also highly rated in 22 other conditions, according to our data. Her clinical expertise encompasses Sturge-Weber Syndrome, Parkes Weber Syndrome, Stork Bite, Epilepsy in Children, and Endovascular Embolization. Dr. Comi is board certified in American Board Of Psychiatry And Neurology.

Megan Bone is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Bone is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Autism Spectrum Disorder, HNRNPH2-Related Disorder, 15q11.2 Microdeletion, and Jacobsen Syndrome.

Carol Greene is a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Greene is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. Her clinical expertise encompasses Musculocontractural Ehlers-Danlos Syndrome (mcEDS), Phenylketonuria (PKU), Increased Head Circumference, and MELAS Syndrome. Dr. Greene is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Xiao Zhou is a primary care provider, practicing in Internal Medicine in Rockville, Maryland. Dr. Zhou is rated as an Advanced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 82 other conditions, according to our data. His clinical expertise encompasses Grix Blankenship Peterson Syndrome, Lacrimo-Auriculo-Dento-Digital Syndrome, Char Syndrome, and Smith-Kingsmore Syndrome.

Perry Foreman is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Foreman is rated as an Advanced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 83 other conditions, according to our data. His clinical expertise encompasses Seizures, Partial Familial Epilepsy, Partial Seizure, Memory Loss, and Gastrostomy.

After completing her bachelors of science degree in biochemistry from the City College of New York (CUNY), Dr. Smith-Hicks entered the Medical Scientist Training Program at Columbia University College of Physicians and Surgeons, where she obtained her M.D., Ph.D. in 2000. She trained in Pediatrics at the Albert Einstein College of Medicine and completed her Neurology and Pediatric Neurology training at the Johns Hopkins University School of Medicine in 2005. Dr. Smith-Hicks trained as a post-doctoral fellow in the Department of Neuroscience at Johns Hopkins University School of Medicine under the guidance of Dr. Paul Worley. She joined the faculty at Kennedy Krieger Institute in 2010 where she now sees patients with Autism Spectrum Disorder and Rett Syndrome, while conducting basic science research exploring disorders of learning and memory. Dr. Smith is rated as an Advanced provider by MediFind in the treatment of Atelosteogenesis Type 1. She is also highly rated in 80 other conditions, according to our data. Her clinical expertise encompasses Rett Syndrome, Ruvalcaba Syndrome, Autism Spectrum Disorder, and Early Infantile Epileptic Encephalopathy. Dr. Smith is board certified in American Board Of Psychiatry And Neurology.

Dr. Gerald Raymond is a clinical geneticist and neurologist at Johns Hopkins where he is also a professor of genetic medicine and neurology. He obtained his MD at the University of Connecticut and was trained in Pediatrics at Johns Hopkins Hospital and Neurology at the Mass. General Hospital. He received additional training in developmental neuropathology at the Universite Catholique de Louvain in Belgium and clinical genetics at the Harvard Program. Dr. Raymond’s research has been at the overlap of genetics and neurology with specific focus on peroxisomal disorders including adrenoleukodystrophy. He has been actively involved in newborn screening for ALD and in developing clinical follow-up programs. He has extensive experience in clinical management of neurogenetic issues including peroxisomal and lysosomal disorders. He presently serves as the Director of the Lysosomal Storage Disease program in the department of Genetic Medicine. Dr. Raymond is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses Adrenoleukodystrophy (ALD), Metachromatic Leukodystrophy, Farber Lipogranulomatosis, and CACH Syndrome. Dr. Raymond is board certified in American Board Of Medical Genetics And Genomics and American Board Of Psychiatry And Neurology.

Eugene Park is a Dermatologist practicing medicine in Baltimore, Maryland. Dr. Park is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. Her clinical expertise encompasses Abruzzo-Erickson Syndrome, Bosma Arhinia Microphthalmia Syndrome, Cockayne Syndrome Type 1, and Townes-Brocks Syndrome. Dr. Park is currently accepting new patients.

Joyce Evans is a primary care provider, practicing in Family Medicine in Columbia, Maryland. Dr. Evans is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses Autonomic Neuropathy, Nevoid Basal Cell Carcinoma Syndrome, Oculodentodigital Dysplasia Dominant, and Allan-Herndon-Dudley Syndrome.

Bilal Sitwat is a Pediatric Neurologist practicing medicine in Baltimore, Maryland. Dr. Sitwat is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Myoclonic Epilepsy, Seizures, West Syndrome, and Epilepsy in Children.

Robert Paschall is a Neurologist practicing medicine in Salisbury, Maryland. Dr. Paschall is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 83 other conditions, according to our data. His clinical expertise encompasses Epilepsy, Stroke, Memory Loss, Seizures, and Gastrostomy.

Joseph Savitt is a Neurologist practicing medicine in Baltimore, Maryland. Dr. Savitt is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 42 other conditions, according to our data. His clinical expertise encompasses Parkinson's Disease, Movement Disorders, Progressive Supranuclear Palsy, Progressive Supranuclear Palsy Atypical, and Gastrostomy.

Tuyet-nhung Nguyen is a primary care provider, practicing in Internal Medicine in Greenbelt, Maryland. Dr. Nguyen is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. Her clinical expertise encompasses Sickle Cell Disease, Osteonecrosis, Chronic Pain, and Type 2 Diabetes (T2D).

Alonso Zea Vera is a Pediatric Neurologist practicing medicine in Silver Spring, Maryland. Dr. Zea Vera is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Tourette Syndrome, Transient Tic Disorder, Chorea, Thrombectomy, and Deep Brain Stimulation.

Melvin Blanchard is a primary care provider, practicing in Internal Medicine in Towson, Maryland. Dr. Blanchard is rated as an Experienced provider by MediFind in the treatment of Atelosteogenesis Type 1. He is also highly rated in 20 other conditions, according to our data. His clinical expertise encompasses Chronic Pain, Maturity Onset Diabetes of the Young, Type 2 Diabetes (T2D), and Hypertension.