| Treatment of ENPP1 Deficiency and ABCC6 Deficiency P Huertas, D Wenkert US Patent App. 18/319,821, 2024 | | 2024 |
| Pyridoxine challenge reflects pediatric hypophosphatasia severity and thereby examines tissue-nonspecific alkaline phosphatase's role in vitamin B6 metabolism MP Whyte, F Zhang, KE Mack, D Wenkert, GS Gottesman, KL Ericson, ... Bone 181, 117033, 2024 | 1 | 2024 |
| Effects of food, fasting, and exercise on plasma pyrophosphate levels and ENPP1 activity in healthy adults G Khursigara, P Huertas, D Wenkert, K O'Brien, Y Sabbagh Bone 171, 116750, 2023 | 1 | 2023 |
| 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 |
| Why are there not more Bayesian clinical trials? Ability to interpret Bayesian and conventional statistics among medical researchers Medical Outreach Team of the Drug Information Association Bayesian ... Therapeutic Innovation & Regulatory Science 57 (3), 426-435, 2023 | 5 | 2023 |
| Evaluating The Effect Of Food, Fasting And Exercise On Inorganic Pyrophosphate (PPi) Levels In Healthy Subjects G Khursigara, P Huertas, D Wenkert, K O’Brien, Y Sabbagh Bone Reports 16, 101313, 2022 | | 2022 |
| MAFB mutations causing multicentric carpotarsal osteolysis disrupt osteoblast and chondrocyte development A Zarei, GS Gottesman, D Wenkert, A Nenninger, S Duan, VN Bijanki, ... Journal of Bone and Mineral Research 37, 171-172, 2022 | 2 | 2022 |
| Eight Adults In Six American Families, Apparently Of Ashkenazi-Jewish Heritage, Presented Biochemical Hallmarks And Clinical Features Of Hypophosphatasia And Carry ALPL Gene … MP Whyte, NSR Neto, JR Starr, N Yalla, F Urano, D Wenkert, S Mumm, ... JOURNAL OF BONE AND MINERAL RESEARCH 37, 218-218, 2022 | | 2022 |
| Hypophosphatasia: Serum Alkaline Phosphatase Activity, Plasma Pyridoxal 5'-Phosphate Levels, And ALPL Gene Findings In Parents Of Affected Children NSR Neto, F Zhang, K Mack, S Mumm, D Wenkert, G Gottesman, ... JOURNAL OF BONE AND MINERAL RESEARCH 37, 162-162, 2022 | | 2022 |
| ENPP1-Deficient Patients Present With Both Skeletal Complications and Ectopic Calcification F Rutsch, Y Nitschke, K Kintzinger, M Hackbarth, U Botschen, R Gafni, ... JOURNAL OF BONE AND MINERAL RESEARCH 37, 248-248, 2022 | | 2022 |
| Why are not there more Bayesian clinical trials? Perceived barriers and educational preferences among medical researchers involved in drug development Medical Outreach Subteam of the Drug Information Association Bayesian ... Therapeutic Innovation & Regulatory Science, 1-9, 2022 | 15 | 2022 |
| Hypophosphatasia: vitamin B6 status of affected children and adults MP Whyte, F Zhang, D Wenkert, KE Mack, VN Bijanki, KL Ericson, ... Bone 154, 116204, 2022 | 12 | 2022 |
| Non-endemic skeletal fluorosis: causes and associated secondary hyperparathyroidism (case report and literature review) FJ Cook, M Seagrove-Guffey, S Mumm, DJ Veis, WH McAlister, VN Bijanki, ... Bone 145, 115839, 2021 | 23 | 2021 |
| Coalescing expansile skeletal disease: delineation of an extraordinary osteopathy involving the IFITM5 mutation of osteogenesis imperfecta type V MP Whyte, J Aronson, WH McAlister, RS Weinstein, D Wenkert, ... Bone 145, 115835, 2021 | 7 | 2021 |
| Utility of genetic testing for prenatal presentations of hypophosphatasia B Sperelakis-Beedham, A Taillandier, C Domingues, M Guberto, E Colin, ... Molecular Genetics and Metabolism 132 (3), 198-203, 2021 | 4 | 2021 |
| X‐linked hypophosphatemia: Uniquely mild disease associated with PHEX 3′‐UTR mutation c.* 231A> G (a retrospective case–control study) PS Smith, GS Gottesman, F Zhang, F Cook, B Ramirez, D Wenkert, ... Journal of Bone and Mineral Research 35 (5), 920-931, 2020 | 18 | 2020 |
| Presentation of a Late Diagnosis of Larsen Syndrome with a Novel Mutation of the Gene Encoding Filamin B (FLNB) D Gupta, D Wenkert JOURNAL OF BONE AND MINERAL RESEARCH 35, 115-116, 2020 | | 2020 |
| Ectonucleotide Pyrosphatase/Phosphodiesterase 1 (ENPP1) Deficiency Appears to be Associated with an Evolving Skeletal Dysplasia in Addition to Ectopic Calcifications and Rickets D Wenkert, W McAlister JOURNAL OF BONE AND MINERAL RESEARCH 35, 291-291, 2020 | | 2020 |
| Vitamin B6 Sufficiency In Children With Hypophosphatasia MP Whyte, F Zhang, D Wenkert, KE Mack, KL Ericson, VN Bijanki, ... JOURNAL OF BONE AND MINERAL RESEARCH 35, 288-288, 2020 | | 2020 |
| Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia MP Whyte, F Zhang, D Wenkert, S Mumm, TJ Berndt, R Kumar Bone 134, 115300, 2020 | 22 | 2020 |