D. Wenkert

发表

Infantile hypophosphatasia: transplantation therapy trial using bone fragments and cultured osteoblasts.

R. Cahill, D. Wenkert, S. Perlman, 2007, The Journal of clinical endocrinology and metabolism.

Deactivating Germline Mutations in LEMD3 Cause Osteopoikilosis and Buschke‐Ollendorff Syndrome, but Not Sporadic Melorheostosis

D. Wenkert, W. Mcalister, S. Mumm, 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Fracture prediction and the definition of osteoporosis in children and adolescents: the ISCD 2007 Pediatric Official Positions.

R. Engelbert, H. Plotkin, L. Dimeglio, 2008, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Bisphosphonate‐Induced Osteopetrosis: Novel Bone Modeling Defects, Metaphyseal Osteopenia, and Osteosclerosis Fractures After Drug Exposure Ceases

D. Wenkert, W. Mcalister, M. Whyte, 2008, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9.

D. Wenkert, W. Mcalister, S. Mumm, 2016, Bone.

PHEX 3′‐UTR c.*231A>G Near The Polyadenylation Signal Is a Relatively Common, Mild, American Mutation That Masquerades as Sporadic or X‐Linked Recessive Hypophosphatemic Rickets

D. Wenkert, W. Mcalister, S. Mumm, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Skeletal changes in epidermal nevus syndrome: Does focal bone disease harbor clues concerning pathogenesis?

M. Cunningham, R. Steiner, C. Heike, 2005, American journal of medical genetics. Part A.

Hypophosphatasia: validation and expansion of the clinical nosology for children from 25 years experience with 173 pediatric patients.

D. Wenkert, S. Coburn, W. Mcalister, 2015, Bone.

Timing of the appearance of macronuclear-specific histone variant hv1 and gene expression in developing new macronuclei of Tetrahymena thermophila

C. Allis, D. Wenkert, 1984, The Journal of cell biology.

X‐Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3′‐UTR Mutation c.*231A>G (A Retrospective Case–Control Study)

D. Wenkert, S. Mumm, M. Whyte, 2020, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia.

R. Kumar, T. Berndt, D. Wenkert, 2020, Bone.

Coalescing Expansile Skeletal Disease: Delineation Of An Extraordinary Osteopathy Involving The IFITM5 Mutation Of Osteogenesis Imperfecta Type V.

H. Plotkin, J. Aronson, S. Duan, 2020, Bone.

Modulation of linker histones during development in Tetrahymena: selective elimination of linker histone during the differentiation of new macronuclei.

J. C. Wiggins, C. Allis, L. Chicoine, 1985, Developmental biology.

Timing ofthe Appearance ofMacron uclear-specific Histone Varianthv1 and Gene Expression inDeveloping New Macronuclei ofTetrahymenathermophila

D. Wenkert, 1984 .

Non-Endemic Skeletal Fluorosis: Causes And Associated Secondary Hyperparathyroidism (Case Report and Literature Review).

D. Wenkert, W. Mcalister, S. Mumm, 2021, Bone.

Chronic Recurrent Multifocal Osteomyelitis Mimicked in Childhood Hypophosphatasia

A. Freemont, D. Wenkert, S. Coburn, 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Hypophosphatasia: Nonlethal disease despite skeletal presentation in utero (17 new cases and literature review)

D. Wenkert, S. Coburn, W. Mcalister, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation.

Philippe M. Campeau, M. Stolina, D. Wenkert, 2020, Bone.

Dysosteosclerosis Presents as an “Osteoclast-Poor” Form of Osteopetrosis: Comprehensive Investigation of a 3-Year-Old Girl and Literature Review

D. Wenkert, W. Mcalister, S. Mumm, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Dual-energy X-ray absorptiometry interpretation: a simple equation for height correction in preteenage children.

D. Wenkert, M. Whyte, Fan Zhang, 2012, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Hypophosphatasia: Vitamin B6 status of affected children and adults.

D. Wenkert, S. Coburn, M. Whyte, 2021, Bone.

Non-lethal hypophosphatasia interpreted as severe skeletal dysplasia in utero

D. Wenkert, S. Coburn, W. Mcalister, 2007 .

Camurati-Engelmann Disease: Unique Variant Featuring a Novel Mutation in TGFβ1 Encoding Transforming Growth Factor Beta 1 and a Missense Change in TNFSF11 Encoding RANK Ligand

W. Totty, D. Wenkert, S. Mumm, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Herpes Zoster Reactivation in Patients With Rheumatoid Arthritis: Analysis of Disease Characteristics and Disease‐Modifying Antirheumatic Drugs

J. Kremer, J. Greenberg, D. Pappas, 2015, Arthritis care & research.

Risk of subsequent fracture after prior fracture among older women

A. Grauer, J. Curtis, D. Wenkert, 2018, Osteoporosis International.

Enzyme-replacement therapy in life-threatening hypophosphatasia.

Nick Bishop, José Luis Millán, Matthew Downs, 2012, The New England journal of medicine.

Bisphosphonate-induced osteopetrosis.

D. Wenkert, W. Mcalister, S. Mumm, 2003, The New England journal of medicine.

Chapter 50 – PRIMARY DISORDERS OF BONE AND CONNECTIVE TISSUES

D. Wenkert, 2011 .

Fibrodysplasia ossificans progressiva: Middle‐age onset of heterotopic ossification from a unique missense mutation (c.974G > C, p.G325A) in ACVR1

D. Wenkert, S. Mumm, M. Whyte, 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Malignancies in children and young adults on etanercept: summary of cases from clinical trials and post marketing reports

D. Wenkert, M. Hooper, Yessenia Bartley, 2013, Pediatric Rheumatology.

A randomized study to evaluate the efficacy and safety of adding topical therapy to etanercept in patients with moderate to severe plaque psoriasis.

M. Lebwohl, J. Koo, D. Wenkert, 2013, Journal of the American Academy of Dermatology.

Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers‐Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders

D. Wenkert, W. Mcalister, S. Mumm, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Absence of MMP2 Mutation in Idiopathic Multicentric Osteolysis with Nephropathy

D. Wenkert, W. Mcalister, S. Mumm, 2007, Clinical orthopaedics and related research.

ASBMR 31st Annual Meeting MO0001–MO0445

Brandi, H. McKay, D. Wenkert, 2009 .

Multicentric carpotarsal osteolysis syndrome is caused by only a few domain‐specific mutations in MAFB, a negative regulator of RANKL‐induced osteoclastogenesis

S. Duan, D. Wenkert, W. Mcalister, 2014, American journal of medical genetics. Part A.

Effects of food, fasting, and exercise on plasma pyrophosphate levels and ENPP1 activity in healthy adults.

G. Khursigara, D. Wenkert, K. O'Brien, 2023, Bone.

Hypophosphatasia: Natural history study of 101 affected children investigated at one research center.

D. Wenkert, M. Whyte, Fan Zhang, 2016, Bone.

Auricular ossification: A newly recognized feature of osteoprotegerin‐deficiency juvenile Paget disease

D. Wenkert, W. Mcalister, S. Mumm, 2016, American journal of medical genetics. Part A.

Utility of genetic testing for prenatal presentations of hypophosphatasia.

E. Colin, A. Zankl, J. Salles, 2021, Molecular genetics and metabolism.

Pregnancy‐Associated Osteoporosis With a Heterozygous Deactivating LDL Receptor‐Related Protein 5 (LRP5) Mutation and a Homozygous Methylenetetrahydrofolate Reductase (MTHFR) Polymorphism

D. Wenkert, S. Mumm, M. Whyte, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Rheumatoid Arthritis Disease Activity and Disability Affect the Risk of Serious Infection Events in RADIUS 1

D. Wenkert, A. Koenig, A. Weaver, 2013, The Journal of Rheumatology.

Congenital blindness and osteoporosis-pseudoglioma syndrome.

M. Trese, D. Wenkert, M. Whyte, 2003, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.