Publications by authors named "Kathryn Dahir"

19Publications

X-Linked Hypophosphatemia: A New Era in Management.

J Endocr Soc 2020 Dec 14;4(12):bvaa151. Epub 2020 Oct 14.

Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.

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December 2020

Multigenerational case examples of hypophosphatasia: Challenges in genetic counseling and disease management.

Mol Genet Metab Rep 2020 Dec 21;25:100661. Epub 2020 Oct 21.

Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.

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December 2020

Pharmacodynamics of asfotase alfa in adults with pediatric-onset hypophosphatasia.

Bone 2021 Jan 26;142:115664. Epub 2020 Sep 26.

Program for Metabolic Bone Disorders at Vanderbilt, Division of Diabetes and Endocrinology, Vanderbilt University Medical Center, Nashville, TN, USA.

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January 2021

Phenotypic Profiling in Subjects Heterozygous for 1 of 2 Rare Variants in the Hypophosphatasia Gene ().

J Endocr Soc 2020 Aug 28;4(8):bvaa084. Epub 2020 Jun 28.

Division of Endocrinology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

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August 2020

Hereditary Hypophosphatemic Rickets with Hypercalciuria (HHRH) Presenting with Genu Valgum Deformity: Treatment with Phosphate Supplementation and Surgical Correction.

Case Rep Endocrinol 2020 9;2020:1047327. Epub 2020 Jul 9.

Division of Diabetes, Endocrinology and Metabolism, Vanderbilt University Medical Center, Nashville, TN, USA.

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July 2020

Burden of Illness in Adults With Hypophosphatasia: Data From the Global Hypophosphatasia Patient Registry.

J Bone Miner Res 2020 Nov 10;35(11):2171-2178. Epub 2020 Aug 10.

Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.

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November 2020

Chronic femoral diaphyseal osteomyelitis with radiographs initially concerning for Paget disease of the bone.

Radiol Case Rep 2020 Apr 27;15(4):344-348. Epub 2020 Jan 27.

Endocrinology and Diabetes, Vanderbilt University Medical Center, 8210 Medical Center East, 1215 21st Avenue South, Nashville, TN 37232-8148, USA.

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April 2020

An intracranial mass causing tumor-induced osteomalacia (TIO): Rapid and complete resolution of severe osteoporosis after surgical resection.

Radiol Case Rep 2020 May 25;15(5):492-497. Epub 2020 Feb 25.

Vanderbilt University Medical Center, Program for Metabolic Bone Disorders at Vanderbilt, Endocrinology and Diabetes, 8210 Medical Center East, 1215 21st Avenue South, Nashville, TN 37232, USA.

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May 2020

Is the Climb Worth the View? The Savings/Alert Ratio for Reducing Vitamin D Testing.

Appl Clin Inform 2020 01 26;11(1):160-165. Epub 2020 Feb 26.

Health Information Technology, Vanderbilt University Medical Center, Nashville, Tennessee, United States.

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January 2020

New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6.

Bone 2019 10 11;127:228-243. Epub 2019 May 11.

Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children - St. Louis, St. Louis, MO 63110, USA; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, MO 63110, USA. Electronic address:

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October 2019

Hypercalcemia secondary to gastrointestinal stromal tumors: parathyroid hormone-related protein independent mechanism?

Endocr Pract 2013 Nov-Dec;19(6):e158-62

Department of Medicine, Division of Diabetes, Endocrinology, and Metabolism, Vanderbilt University Medical Center, Nashville, Tennessee.

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July 2014

Sodium thiosulfate in the treatment of non-uremic calciphylaxis.

J Dermatol 2013 Aug 10;40(8):649-52. Epub 2013 May 10.

Division of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-2600, USA.

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August 2013

Differentiating familial hypocalciuric hypercalcemia from primary hyperparathyroidism.

Endocr Pract 2013 Jul-Aug;19(4):697-702

Division of Surgical Oncology and Endocrine Surgery, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA.

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March 2014

Treatment of adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a clinical practice audit.

Endocr Pract 2003 Sep-Oct;9(5):347-52

Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

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April 2004