Michael A. Levine

Endocrinology
3401 Civic Center Blvd
Philadelphia, PA 19104

Last Updated: 09/26/2026

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Found 144 publications

The impact of parathyroid hormone replacement with palopegteriparatide on synthesis of 1,25-dihydroxy vitamin D in hypoparathyroidism.

The impact of parathyroid hormone replacement with palopegteriparatide on synthesis of 1,25-dihydroxy vitamin D in hypoparathyroidism.

Journal: Expert review of clinical pharmacology
Published: August 17, 2026

Palopegteriparatide Therapy for Hypoparathyroidism: Targeting the PTH Receptor Rouses the Sleeping Skeleton.

Palopegteriparatide Therapy for Hypoparathyroidism: Targeting the PTH Receptor Rouses the Sleeping Skeleton.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: March 30, 2026

Hypoparathyroidism: translating science from the laboratory to the clinic.

Hypoparathyroidism: translating science from the laboratory to the clinic.

Journal: The lancet. Diabetes & endocrinology
Published: March 25, 2026

Understanding the Periodontitis-Diabetes Linkage: Mechanisms and Evidence.

Understanding the Periodontitis-Diabetes Linkage: Mechanisms and Evidence.

Journal: Journal of dental research
Published: November 26, 2025

Liver-directed base editing of ABCC6 prevents ectopic calcification in a variant-humanized mouse model of pseudoxanthoma elasticum.

Liver-directed base editing of ABCC6 prevents ectopic calcification in a variant-humanized mouse model of pseudoxanthoma elasticum.

Journal: Molecular therapy. Nucleic acids
Published: September 27, 2025

Health-related quality of life in a cohort of 1070 patients with hypoparathyroidism.

Health-related quality of life in a cohort of 1070 patients with hypoparathyroidism.

Journal: European journal of endocrinology
Published: March 13, 2025

Unusual PHEX variants implicate uncommon genetic mechanisms for X-linked hypophosphatemic rickets.

Unusual PHEX variants implicate uncommon genetic mechanisms for X-linked hypophosphatemic rickets.

Journal: JBMR plus
Published: November 01, 2024

Clinical evaluation and molecular analysis of genetic and epigenetic inactivation defects in GNAS in children: A multicenter experience in China.

Clinical evaluation and molecular analysis of genetic and epigenetic inactivation defects in GNAS in children: A multicenter experience in China.

Journal: European journal of endocrinology
Published: October 23, 2024

Quantitative hypermorphic FAM111A alleles cause autosomal recessive Kenny-Caffey syndrome type 2 and osteocraniostenosis.

Quantitative hypermorphic FAM111A alleles cause autosomal recessive Kenny-Caffey syndrome type 2 and osteocraniostenosis.

Journal: JCI insight
Published: September 10, 2024

Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1B.

Recurrent small variants in NESP55/NESPAS associated with broad GNAS methylation defects and pseudohypoparathyroidism type 1B.

Journal: JCI insight
Published: August 22, 2024

An activating calcium-sensing receptor variant with biased signaling reveals a critical residue for Gα11 coupling.

An activating calcium-sensing receptor variant with biased signaling reveals a critical residue for Gα11 coupling.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: July 19, 2024

Clinical Efficacy of Zoledronic Acid on Fracture Reduction in Youth With Primary and Secondary Skeletal Fragility.

Clinical Efficacy of Zoledronic Acid on Fracture Reduction in Youth With Primary and Secondary Skeletal Fragility.

Journal: The Journal of clinical endocrinology and metabolism
Published: July 04, 2024
Showing 1-12 of 144

Last Updated: 09/26/2026