Publications by authors named "Kathryn Dahir"

19Publications

X-Linked Hypophosphatemia: A New Era in Management.

Authors:
Kathryn Dahir Mary Scott Roberts Stan Krolczyk Jill H Simmons

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.

Authors:
Erin Huggins Ricardo Ong Cheryl Rockman-Greenberg Lauren Bailey Flueckinger Kathryn M Dahir Priya S Kishnani

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

Characterization of physical, functional, and cognitive performance in 15 adults with hypophosphatasia.

Authors:
Christina Durrough Juan M Colazo Jill Simmons Jiun-Ruey Hu Margaret Hudson Margo Black Michael de Riesthal Kathryn Dahir

Bone 2021 Jan 16;142:115695. Epub 2020 Oct 16.

Vanderbilt University Medical Center, Nashville, TN, USA. Electronic address:

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January 2021

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

Authors:
Lothar Seefried Priya S Kishnani Scott Moseley Andrew E Denker Eric Watsky Michael P Whyte Kathryn M Dahir

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 ().

Authors:
Daniel R Tilden Jonathan H Sheehan John H Newman Jens Meiler John A Capra Andrea Ramirez Jill Simmons Kathryn Dahir

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.

Authors:
Juan M Colazo Seth A Reasoner Ginger Holt Marie C M Faugere Kathryn M Dahir

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.

Authors:
Lothar Seefried Kathryn Dahir Anna Petryk Wolfgang Högler Agnès Linglart Gabriel Ángel Martos-Moreno Keiichi Ozono Shona Fang Cheryl Rockman-Greenberg Priya S Kishnani

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.

Authors:
Seth A Reasoner Juan M Colazo Jonathan Tucci Justin Cates Kathryn M Dahir

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.

Authors:
Juan M Colazo Reid C Thompson Natalie V Covington Kathryn M Dahir

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.

Authors:
Chase D Hendrickson Michael F McLemore Kathryn M Dahir Shari Just Zahra Shajani-Yi Joseph LeGrand Christoph U Lehmann Asli Weitkamp

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.

Authors:
Michael P Whyte William H McAlister Fan Zhang Vinieth N Bijanki Angela Nenninger Gary S Gottesman Elizabeth L Lin Margaret Huskey Shenghui Duan Kathryn Dahir Steven Mumm

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

Metabolic and Endocrine Disorders in Pseudarthrosis.

Authors:
Jeffrey M Hills Inamullah Khan Kristin R Archer Ahilan Sivaganesan Joshua Daryoush Daniel Y Hong Kathryn M Dahir Clinton J Devin Byron Stephens

Clin Spine Surg 2019 06;32(5):E252-E257

Departments of Orthopaedics and Rehabilitation.

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June 2019

Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine Disorders.

Authors:
Kathryn M Dahir Daniel R Tilden Jeremy L Warner Lisa Bastarache Derek K Smith Aliya Gifford Andrea H Ramirez Jill S Simmons Margo M Black John H Newman Josh C Denny

J Clin Endocrinol Metab 2018 06;103(6):2234-2243

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.

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June 2018

Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa.

Authors:
Priya S Kishnani Eric T Rush Paul Arundel Nick Bishop Kathryn Dahir William Fraser Paul Harmatz Agnès Linglart Craig F Munns Mark E Nunes Howard M Saal Lothar Seefried Keiichi Ozono

Mol Genet Metab 2017 09 25;122(1-2):4-17. Epub 2017 Jul 25.

Department of Pediatrics, Osaka University, Suita, Osaka 565-0871, Japan.

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September 2017

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

Authors:
Prathima Jasti Vipul Tulsi Lakhani Alison Woodworth Kathryn McCrystal Dahir

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.

Authors:
Matthew S Ning Kathryn M Dahir Emily H Castellanos Laura Y McGirt

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.

Authors:
Myrick C Shinall Kathryn McCrystal Dahir James T Broome

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

Ectopic adrenocorticotropic hormone hypersecretion due to a primary pulmonary paraganglioma.

Authors:
Kathryn McCrystal Dahir Adriana Gonzalez Monica P Revelo S Rafeeq Ahmed John R Roberts Lewis S Blevins

Endocr Pract 2004 Sep-Oct;10(5):424-8

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

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April 2005

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

Authors:
Howard Y Li Kathryn McCrystal Dahir Lewis S Blevins

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