Zobrazeno 1 - 10
of 58
pro vyhledávání: '"M Dahir"'
Autor:
Saido Gedi, Abdirahim Mohamed Hassan, Mohamoud M. Dahir, Abubakar Ahmed, Nasra Abdulsamad Mohamud, Bashiru Garba, Chukwuma David Umeokonkwo, Mohamed Abdelrahman Mohamed
Publikováno v:
BMC Oral Health, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Oral diseases remain a significant public health problem worldwide despite being largely preventable. Oral disorders such as dental caries, periodontal diseases, and oral cancers are highly prevalent chronic conditions that negati
Externí odkaz:
https://doaj.org/article/140413234e8f459ea1a7797df0ff6ebe
Autor:
Priya S. Kishnani, Gabriel Ángel Martos-Moreno, Agnès Linglart, Anna Petryk, Andrew Messali, Shona Fang, Cheryl Rockman-Greenberg, Keiichi Ozono, Wolfgang Högler, Lothar Seefried, Kathryn M. Dahir
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Hypophosphatasia (HPP) is a rare inherited disease caused by deficient activity of tissue-nonspecific alkaline phosphatase. Many adults with HPP have a high burden of disease, experiencing chronic pain, fatigue, limited mobility,
Externí odkaz:
https://doaj.org/article/37968c05241044a7ae66037fae804ebb
Publikováno v:
Case Reports in Rheumatology, Vol 2024 (2024)
Objectives. Rare metabolic bone diseases can present with symptoms mimicking more common rheumatological conditions including spondyloarthritis, osteoarthritis, and fibromyalgia. Increasing awareness of these rare diseases within the rheumatology com
Externí odkaz:
https://doaj.org/article/3d65abb7cf024d38b6e4394fe4ff15e2
Autor:
Juan M. Colazo, Julia Quirion, Anthony D. Judice, Jennifer Halpern, Herbert S. Schwartz, S. Bobo Tanner, Joshua M. Lawrenz, Kathryn M. Dahir, Ginger E. Holt
Publikováno v:
Bone Reports, Vol 19, Iss , Pp 101715- (2023)
Background: Metabolic bone diseases (MBD) are typically diagnosed by non-invasive imaging and clinical biomarkers. However, imaging does not provide structural information, and biomarkers can be transiently affected by many systemic factors. Bone bio
Externí odkaz:
https://doaj.org/article/728dce1dcd3644dc9deb28f78acda3ab
Autor:
Kathryn M. Dahir, Lothar Seefried, Priya S. Kishnani, Anna Petryk, Wolfgang Högler, Agnès Linglart, Gabriel Ángel Martos-Moreno, Keiichi Ozono, Shona Fang, Cheryl Rockman-Greenberg
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background The clinical signs and symptoms of hypophosphatasia (HPP) can manifest during any stage of life. The age at which a patient’s symptoms are reported can impact access to targeted treatment with enzyme replacement therapy (asfotas
Externí odkaz:
https://doaj.org/article/3b71631dff824edd8fcf1b9f203f0927
Autor:
Kathryn M. Dahir, Priya S. Kishnani, Gabriel Ángel Martos-Moreno, Agnès Linglart, Anna Petryk, Cheryl Rockman-Greenberg, Samantha E. Martel, Keiichi Ozono, Wolfgang Högler, Lothar Seefried
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionHypophosphatasia (HPP) manifests in adults as fractures/pseudofractures, pain, muscle weakness, and other functional impairments. Better phenotypic disease characterization is needed to help recognize disability and treat patients with HP
Externí odkaz:
https://doaj.org/article/5e063fc646ab473a8ee30714e836a6df
Autor:
Juan M. Colazo, BSc, Joseph A. DeCorte, BS, Erin A. Gillaspie, MD, MPH, Andrew L. Folpe, MD, Kathryn M. Dahir, MD
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 100744- (2021)
Tumor-induced osteomalacia (TIO), caused by phosphaturic mesenchymal tumors (PMTs), is a rare paraneoplastic syndrome characterized by frequent bone fractures, bone pain, muscle weakness, and affected gait. These tumors typically secrete high levels
Externí odkaz:
https://doaj.org/article/ce3ae98c10d64f2395f285204805e65c
Autor:
Erin Huggins, Ricardo Ong, Cheryl Rockman-Greenberg, Lauren Bailey Flueckinger, Kathryn M. Dahir, Priya S. Kishnani
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100661- (2020)
Hypophosphatasia (HPP) is an inherited metabolic condition caused by pathogenic mutations in the ALPL gene. This leads to deficiency of tissue non-specific alkaline phosphatase (TNSALP), resulting in decreased mineralization of the bones and/or teeth
Externí odkaz:
https://doaj.org/article/843550e0946b43caa1256de132eeb1ee
Publikováno v:
Case Reports in Endocrinology, Vol 2020 (2020)
We describe a case of hereditary hypophosphatemic rickets with hypercalciuria (HHRH) in a 32-year-old female with short stature, chronic pathologic genu valgum deformity, and knee pain who was referred to endocrinology clinic after previous inconclus
Externí odkaz:
https://doaj.org/article/8c1c369647b64207a56b2619d86d5fc0
Publikováno v:
The Journal of Sexual Medicine. 20
Introduction Vulvodynia is associated with significant burden and impaired quality of life and affects up to 28% of women of reproductive age. The most common subtype is provoked vestibulodynia (PVD), in which pain is localized and triggered by vesti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ab7b0b6988c306df344656f7e7afb71
https://doi.org/10.1093/jsxmed/qdad061.082
https://doi.org/10.1093/jsxmed/qdad061.082