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Mary Scott Ramnitz

National Institutes of Health

13

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225

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Hypercementosis Associated with ENPP1 Mutations and GACI

2018 Journal of Dental Research
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Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature

2018 Osteoporosis International
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A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers

2016 European Journal of Pediatrics
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Phenotypic and Genotypic Characterization and Treatment of a Cohort with Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome

2016
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Phenotypic and Genotypic Characterization and Treatment of a Cohort With Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome

2016 Journal of Bone and Mineral Research
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Nephrogenic Diabetes Insipidus with Partial Response to Ddavp Caused by a Novel AVPR2 Splice Site Mutation

2015
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Benign vaginal bleeding in 24 prepubertal patients: Clinical, biochemical and imaging features

2014 Journal of Pediatric Endocrinology and Metabolism
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Pituitary stalk lesion in a 13-year-old female.

2014 Journal of Pediatric Endocrinology and Metabolism
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Bone densitometry in children and adolescents.

2014 Current Opinion in Obstetrics & Gynecology
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Rare Bone Diseases and Their Dental, Oral, and Craniofacial Manifestations

2014 Journal of Dental Research
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Citations (79)