Author/Creator: Wenkert, Deborah - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Wenkert, Deborah

1. Auricular ossification: A newly recognized feature of osteoprotegerin‐deficiency juvenile Paget disease. Issue 4 (14th January 2016)

Authors:: Gottesman, Gary S.; Madson, Katherine L.; McAlister, William H.; Nenninger, Angela; Wenkert, Deborah; Mumm, Steven; Whyte, Michael P.
Journal:: American journal of medical genetics
Issue:: Volume 170:Issue 4(2016)
Page Start:: 978
Record Type:: Journal Article
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2. Herpes Zoster Reactivation in Patients With Rheumatoid Arthritis: Analysis of Disease Characteristics and Disease‐Modifying Antirheumatic Drugs. Issue 12 (December 2015)

Authors:: Pappas, Dimitrios A.; Hooper, Michele M.; Kremer, Joel M.; Reed, George; Shan, Ying; Wenkert, Deborah; Greenberg, Jeffrey D.; Curtis, Jeffrey R.
Journal:: Arthritis care & research
Issue:: Volume 67:Issue 12(2015:Dec.)
Page Start:: 1671
Record Type:: Journal Article
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3. Multicentric carpotarsal osteolysis syndrome is caused by only a few domain‐specific mutations in MAFB, a negative regulator of RANKL‐induced osteoclastogenesis. Issue 9 (2nd July 2014)

Authors:: Mumm, Steven; Huskey, Margaret; Duan, Shenghui; Wenkert, Deborah; Madson, Katherine L.; Gottesman, Gary S.; Nenninger, Angela R.; Laxer, Ronald M.; McAlister, William H.; Whyte, Michael P.
Journal:: American journal of medical genetics
Issue:: Volume 164:Issue 9(2014.)
Page Start:: 2287
Record Type:: Journal Article
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4. 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. (January 2015)

Authors:: Mumm, Steven; Huskey, Margaret; Cajic, Adela; Wollberg, Valerie; Zhang, Fan; Madson, Katherine L; Wenkert, Deborah; McAlister, William H; Gottesman, Gary S; Whyte, Michael P
Journal:: Journal of bone and mineral research
Issue:: Volume 30:Number 1(2015:Jan.)
Page Start:: 137
Record Type:: Journal Article
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5. Pregnancy‐Associated Osteoporosis With a Heterozygous Deactivating LDL Receptor‐Related Protein 5 (LRP5) Mutation and a Homozygous Methylenetetrahydrofolate Reductase (MTHFR) Polymorphism. (April 2014)

Authors:: Cook, Fiona J; Mumm, Steven; Whyte, Michael P; Wenkert, Deborah
Journal:: Journal of bone and mineral research
Issue:: Volume 29:Number 4(2014:Apr.)
Page Start:: 922
Record Type:: Journal Article
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6. X‐Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3′‐UTR Mutation c.*231A>G (A Retrospective Case–Control Study). (10th March 2020)

Authors:: Smith, Pamela S; Gottesman, Gary S; Zhang, Fan; Cook, Fiona; Ramirez, Beatriz; Wenkert, Deborah; Wollberg, Valerie; Huskey, Margaret; Mumm, Steven; Whyte, Michael P
Journal:: Journal of bone and mineral research
Issue:: Volume 35:Number 5(2020)
Page Start:: 920
Record Type:: Journal Article
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