Debra Counts is a Pediatric Endocrinologist in Baltimore, Maryland. Dr. Counts is rated as a Distinguished provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Idiopathic Short Stature (ISS), Short Stature (Growth Disorders), Klinefelter Syndrome, and Pediatric Growth Hormone Deficiency.

Dr. Dobs is presently an active clinical researcher in the field of endocrine gonadal function. She is particularly interested in new forms of male hormone replacement therapy and has published extensively in the area of hormonal changes with aging and chronic disease. Her clinical practice covers general endocrinology, with a focus on sex hormone disorders in both men and women. As Director of the Johns Hopkins Clinical Research Network, she oversees a multi-institutional consortium of hospitals in the mid-Atlantic states dedicated to facilitating clinical research through an academic-community hospital partnership. Dr. Dobs is rated as an Advanced provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Hypogonadism, Eunuchoidism Familial Hypogonadotropic, Testicular Failure, Isolated Hypogonadotropic Hypogonadism, and Hormone Replacement Therapy (HRT).

Dr. Herati is a urologist with fellowship training in male infertility and andrology. He has specialized training to perform complex reconstructions of the reproductive system, including vasectomy reversal with vasovasostomy and vasoepididymostomy. Additionally, he has an interest in treating patients with chronic prostatitis and pelvic pain, as well as patients experiencing low testosterone, erectile dysfunction, Peyronie’s disease and benign prostatic hyperplasia (BPH). Of note, he has the ability to perform fertility treatments on patients who have experienced spinal cord injuries using nonsurgical methods of sperm extraction. Dr. Herati believes in an individualized approach to care that addresses the whole patient. He invests significant time into building a rapport with his patients so that they feel comfortable opening up about these issues, allowing him to accurately identify and manage each patient’s needs. His research interests include decoding the genetic basis of male infertility, investigating the impact of referred pain from peripheral nerves to the bladder, and characterizing the effects of low testosterone on prostate inflammation and PSA screening. Dr. Herati sees patients at both the Johns Hopkins Hospital and The Johns Hopkins Bayview Medical Center. Videos Amin Herati, M.D.Urologist. Dr. Herati is rated as an Advanced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Enlarged Prostate (BPH), Varicocele, Hypogonadism, Nephrectomy, and Prostatectomy.

Vikram Shenoy, M.D., practices endocrinology at Johns Hopkins Community Physicians Downtown Bethesda. He received his medical degree from University of Connecticut School of Medicine, and also completed his residency in endocrinology at Hospital of the University of Pennsylvania. He practices general endocrinology, including the treatment of thyroid disorders, diabetes, PCOS, pituitary and adrenal disorders, hypogonadism and osteoporosis. Dr. Shenoy is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Type 1 Diabetes (T1D), and Hypothyroidism.

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 Klinefelter Syndrome. His top areas of expertise are Epicanthal Folds, Strabismus, Brown Syndrome, and Hypotonia.

Dr. Malinda Wu is a pediatric endocrinologist seeing patients at the Johns Hopkins Children’s Center in Baltimore, Maryland. She specializes in a wide range of pediatric endocrine conditions including metabolic bone disease, pediatric osteoporosis and cystic fibrosis endocrinopathies. Dr. Wu received her M.D. from Jefferson Medical College, Thomas Jefferson University. She completed pediatrics residency at Penn State Hershey Medical Center and her pediatric endocrine fellowship at Emory University School of Medicine. She received her Master of Science in Clinical Research from Emory University (2021). Dr. Wu has been a faculty member at Johns Hopkins since 2021. Dr. Wu’s research interests are in metabolic bone disease and the health of women with cystic fibrosis. Dr. Wu’s current research is focused on women with cystic fibrosis and how estrogen supplementation may impact their health. She has received grant funding from the Cystic Fibrosis Foundation. Dr. Wu is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Osteogenesis Imperfecta, Hypogonadism, Malnutrition, Exocrine Pancreatic Insufficiency, and Hormone Replacement Therapy (HRT).

David Fenig is a Urologist in Columbia, Maryland. Dr. Fenig is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Male Pseudohermaphroditism with Gynecomastia, Eunuchoidism Familial Hypogonadotropic, Testicular Failure, Hypogonadism Primary Partial Alopecia, and Ureteroscopy.

Dr. David W. Cooke is an associate professor of pediatrics at the Johns Hopkins University School of Medicine. Dr. Cooke’s clinical activities include both a general pediatric endocrine clinic and a pediatric diabetes clinic. His clinical interests include all endocrine disorders in children and adolescents, including short stature, abnormal pubertal development, growth hormone dysregulation, thyroid disorders, hormone deficiencies, hypopituitarism, diabetes insipidis, pituitary adenoma, prolactinoma, goiter, Cushing's disease, Addison's disease, polycystic ovary syndrome, congenital adrenal hyperplasia and disorders of sexual differentiation, Turner syndrome and Klinefelter syndrome, among others. He serves as clinical director of the division of pediatric endocrinology and director of the Pediatric Endocrinology Fellowship Training Program at Johns Hopkins. He is a member of the Johns Hopkins Klinefelter Syndrome Center. Dr. Cooke completed his undergraduate studies at the Massachusetts Institute of Technology, and received his medical degree from the Duke University School of Medicine. He then completed his residency in pediatrics at The Johns Hopkins Hospital, where he also completed a fellowship in pediatric endocrinology. He has been a faculty member in the Division of Pediatric Endocrinology at the Johns Hopkins since 1993. After his fellowship, Dr. Cooke spent five years of additional research training in the Department of Biological Chemistry at Johns Hopkins, supported by an individual Physician Scientist Award from the National Institutes of Health (NIH). Dr. Cooke’s past research interest was the molecular basis of insulin resistance and obesity, with studies examining the role the adipocyte plays in these conditions. He had received research funding for these studies from the NIH and from the American Diabetes Association. Dr. Cooke is a recipient of the Johns Hopkins University School of Medicine Institute for Excellence in Education award for Outstanding Achievement in Medical and Biomedical Education. He also has been recognized as a Top Doctor by Baltimore magazine. Dr. Cooke is a member of the Society for Pediatric Research, the American Diabetes Association, the Endocrine Society and Pediatric Endocrinology Society. He is a fellow of the American Academy of Pediatrics. Dr. Cooke is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Klinefelter Syndrome, Type 1 Diabetes (T1D), Precocious Puberty, and Diabetic Ketoacidosis.

Melissa Pagan is a Pediatrics provider in Baltimore, Maryland. Dr. Pagan is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), Familial Short Stature (FSS), and Precocious Puberty.

Kayur Bhavsar is an Endocrinologist in Frederick, Maryland. Dr. Bhavsar is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Type 2 Diabetes (T2D), Thyroid Nodule, Hypothyroidism, and Hypercalcemia.

Ryan Miller is a Pediatric Endocrinologist in Baltimore, Maryland. Dr. Miller is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), Familial Short Stature (FSS), and Precocious Puberty.

Mansur Shomali is an Endocrinologist in Baltimore, Maryland. Dr. Shomali is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Paget's Disease of Bone, and Type 1 Diabetes (T1D).

Salman Bhat is an Endocrinologist in Salisbury, Maryland. Dr. Bhat is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Type B Insulin Resistance Syndrome, Type 2 Diabetes (T2D), Low Blood Sugar, and Thyroid Storm.

Paula Newton is a Pediatric Endocrinologist in Baltimore, Maryland. Dr. Newton is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), Familial Short Stature (FSS), and Precocious Puberty.

Dominique Long is a Pediatric Endocrinologist in Baltimore, Maryland. Dr. Long is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Short Stature (Growth Disorders), Familial Short Stature (FSS), Idiopathic Short Stature (ISS), and Panhypopituitarism.

Nejat Naser is a primary care provider, practicing in Endocrinologist in Largo, Maryland. Dr. Naser is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Type 1 Diabetes (T1D), Thyroid Storm, Hyperthyroidism, and Graves Disease.

Tadele Desalew is an Endocrinologist in Waldorf, Maryland. Dr. Desalew is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Type 2 Diabetes (T2D), Hypothyroidism, Thyroid Storm, and Hyperthyroidism.

Maximilian Muenke is a Medical Genetics provider in Bethesda, Maryland. Dr. Muenke is rated as an Advanced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Holoprosencephaly, Turner Syndrome, Craniosynostosis, and Corpus Callosum Agenesis.

Pim Suwannarat is a Medical Genetics specialist and a Pediatrics provider in Suitland, Maryland. Dr. Suwannarat is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. Her top areas of expertise are Triple X Syndrome, Classic Galactosemia, Ehlers-Danlos Syndrome (EDS), and Chromosome 10q Deletion. Dr. Suwannarat is currently accepting new patients.

Charles Benner is a primary care provider, practicing in Geriatrics and Internal Medicine in Solomons, Maryland. Dr. Benner is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His top areas of expertise are Dementia, Glucocorticoid-Remediable Aldosteronism, Familial Hypertension, and Hypertension. Dr. Benner is currently accepting new patients.