| 2002-04 Vs. 2007-09: Initiation of Combination, and Tapering/Discontinuation (DC) Patterns of TNFi and MTX in a US (RA) Patient Registry: Analysis with CDAI Scores. D Wenkert, S Grant, DH Collier, AS Koenig, JM Kremer ARTHRITIS AND RHEUMATISM 64 (10), S167-S168, 2012 | | 2012 |
| A new pediatric sclerosing bone disorder featuring fragility fractures. P Tebben, D Wenkert, DV Novack, LA DiMeglio, H Sedighi, W McAlister, ... JOURNAL OF BONE AND MINERAL RESEARCH 21, S432-S432, 2006 | 2 | 2006 |
| A Phase 1/2, Open-Label, Multiple Ascending Dose Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of INZ-701 in Adults with ENPP1 … R Wermers, R Fuhr, D Schnabel, T Arnason, A Bensacon, B Cizman, ... Endocrine Abstracts 90, 2023 | | 2023 |
| A randomized study to evaluate the efficacy and safety of adding topical therapy to etanercept in patients with moderate to severe plaque psoriasis MG Lebwohl, L Kircik, KC Duffin, D Pariser, M Hooper, D Wenkert, ... Journal of the American Academy of Dermatology 69 (3), 385-392, 2013 | 32 | 2013 |
| A unique, autosomal dominant, bone and dental dysplasia in a 4-generation American kindred. D Wenkert, WH McAlister, DV Novack, H Sedighi, M Horwith, MP Whyte JOURNAL OF BONE AND MINERAL RESEARCH 21, S430-S430, 2006 | | 2006 |
| AB0472 The frequency of methotrexate (MTX) or prednisone discontinuation and of TNF inhibitor (TNFI) discontinuation/switching in rheumatoid arthritis (RA) patients results … J Kremer, D Wenkert, S Grant, P Xu, A Koenig, D Collier Annals of the Rheumatic Diseases 71 (Suppl 3), 664-664, 2013 | | 2013 |
| Absence of MMP2 mutation in idiopathic multicentric osteolysis with nephropathy D Wenkert, S Mumm, SM Wiegand, WH McAlister, MP Whyte Clinical Orthopaedics and Related Research® 462, 80-86, 2007 | 15 | 2007 |
| Absence of MMP2 mutations in idiopathic multicentric osteolysis with nephropathy in 2 American boys. D Wenkert, S Mumn, SM Wiegand, WH McAlister, MP Whyte ARTHRITIS AND RHEUMATISM 52 (9), S304-S304, 2005 | | 2005 |
| Acquired osteopetrosis D Wenkert JOURNAL OF BONE AND MINERAL RESEARCH 19 (8), 1373-1373, 2004 | | 2004 |
| Additional Clinical Features of Idiopathic Multicentric Osteolysis with Nephropathy (OMIM% 166300). D Wenkert, WH McAlister, MP Whyte JOURNAL OF BONE AND MINERAL RESEARCH 23, S293-S293, 2008 | 1 | 2008 |
| Antigen induced arthritis in IL1 beta deficient mice. D Wenkert, DD Chaplin ARTHRITIS AND RHEUMATISM 40 (9), 895-895, 1997 | | 1997 |
| Arzneimittelsicherheit in der Kinderrheumatologie K Minden, J Klotsche, M Niewerth, G Horneff, A Zink Arthritis und Rheuma 34 (01), 42-47, 2014 | | 2014 |
| Aspirin-responsive, expansile bone disease with asplenism: A new autosomal dominant entity. D Wenkert, WH McAlister, S Mumm, MP Whyte JOURNAL OF BONE AND MINERAL RESEARCH 18, S388-S388, 2003 | | 2003 |
| Auricular ossification: A newly recognized feature of osteoprotegerin‐deficiency juvenile Paget disease GS Gottesman, KL Madson, WH McAlister, A Nenninger, D Wenkert, ... American Journal of Medical Genetics Part A 170 (4), 978-985, 2016 | 14 | 2016 |
| Bisphosphonate-induced osteopetrosis MP Whyte, D Wenkert, KL Clements, WH McAlister, S Mumm New England Journal of Medicine 349 (5), 457-463, 2003 | 523 | 2003 |
| Bisphosphonate‐induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceases MP Whyte, WH McAlister, DV Novack, KL Clements, PL Schoenecker, ... Journal of Bone and Mineral Research 23 (10), 1698-1707, 2008 | 110 | 2008 |
| Bisphosphonates in children with bone diseases-Reply MP Whyte, D Wenkert, WH McAlister NEW ENGLAND JOURNAL OF MEDICINE 349 (21), 2069-2071, 2003 | 1 | 2003 |
| Bone mineral density assessed by DEXA does not improve spontaneously during puberty in girls with untreated mild osteogenesis imperfecta. D Wenkert, MN Podgornik, WH McAlister, WH Whyte JOURNAL OF BONE AND MINERAL RESEARCH 17, S384-S384, 2002 | | 2002 |
| Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation S Mumm, GS Gottesman, D Wenkert, PM Campeau, A Nenninger, ... Bone 130, 115047, 2020 | 23 | 2020 |
| Bruck syndrome variant lacking congenital contractures due to novel compound heterozygous PLOD2 mutations S Mumm, GS Gottesman, PM Campeau, A Nenninger, M Huskey, ... JOURNAL OF BONE AND MINERAL RESEARCH 33, 182-182, 2018 | 1 | 2018 |