Overview
Xinying Hong is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Hong is rated as an Advanced provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Krabbe Disease, Leukodystrophy, Mucopolysaccharidoses (MPS), and Multiple Sulfatase Deficiency.
Her clinical research consists of co-authoring 37 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Multiple Sulfatase Deficiency.
Insurance
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Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Childrens Health Care Associates Inc
Rebecca Ahrens-Nicklas is a Pediatrics specialist and a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Ahrens-Nicklas is rated as an Elite provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Multiple Sulfatase Deficiency, Cardiomyopathic Lentiginosis, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, and Noonan Syndrome.
Childrens Health Care Associates Inc
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ficicioglu is rated as a Distinguished provider by MediFind in the treatment of Multiple Sulfatase Deficiency. His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
Penn Translational Medicine And Human Genetics
Staci Kallish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kallish is rated as a Distinguished provider by MediFind in the treatment of Multiple Sulfatase Deficiency. Her top areas of expertise are Neurofibromatosis Type 1 (NF1), Gaucher Disease Type 1, Fabry Disease, and Neurofibromatosis.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Cholesteryl Ester Storage Disease
- Glutaric Acidemia Type 1Dr. Hong isAdvanced. Learn about Glutaric Acidemia Type 1.
- Krabbe DiseaseDr. Hong isAdvanced. Learn about Krabbe Disease.
- LeukodystrophyDr. Hong isAdvanced. Learn about Leukodystrophy.
- Lysosomal Acid Lipase Deficiency
- Mucolipidosis Type 4Dr. Hong isAdvanced. Learn about Mucolipidosis Type 4.
- Experienced
- Adrenoleukodystrophy (ALD)Dr. Hong isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Alpha MannosidosisDr. Hong isExperienced. Learn about Alpha Mannosidosis.
- Batten DiseaseDr. Hong isExperienced. Learn about Batten Disease.
- Biotinidase DeficiencyDr. Hong isExperienced. Learn about Biotinidase Deficiency.
- Classic GalactosemiaDr. Hong isExperienced. Learn about Classic Galactosemia.
- CLN1 DiseaseDr. Hong isExperienced. Learn about CLN1 Disease.