Results 181 to 190 of about 9,342 (275)

THU458 Demineralization Zebras: A Rare Case Of Hypophosphatasia In An Adult Presenting With Osteopenia

, 2023
Bhanvi Prakash Ramchandani, Aysha Habib Khan, Hassaan Aftab   +2 more
openalex   +1 more source

Brief Clinical Report: Hypophosphatasia—Diagnostic Considerations and Treatment Outcomes in an Infant [PDF]

, 2018
Sara H. Duffus, Bradly J. Thrasher, Ali S. Çalıkoğlu   +2 more
openalex   +1 more source

Corrigendum to "Multigenerational genetic inheritance and clinical characteristics of the rare disease hypophosphatasia in 6 families: A case series" [Bone Rep. 26 (2025) 1-6 (101857)]. [PDF]

Bone Rep
Kannu P, Khan AA, Francis M, Adachi JD.
europepmc   +1 more source

Change in fracture rate and healthcare resource utilization among patients with hypophosphatasia following initiation of asfotase alfa: a retrospective US claims database analysis. [PDF]

JBMR Plus
Lyons G, Bates T, Vlasnik J, Wakeford C, Donckels EA, Chan PK, Robinson SB, Dahir KM.   +7 more
europepmc   +1 more source

Neonatal Multiple Bone Fractures: A Case Report of Hypophosphatasia. [PDF]

Case Rep Endocrinol
Homyani DKA, Hemaiani SKA, Harthi QQA, Zahrani RA, Qarni ASA.   +4 more
europepmc   +1 more source

Hypophosphatasia: 90 Years from a Canadian Discovery-A Comprehensive Review of the <i>ALPL</i> Gene Underlying Rathbun's Syndrome. [PDF]

Genes (Basel)
Sergi CM.
europepmc   +1 more source

MON-496 Bone Mineral Density improvement with Vitamin Dsupplementation in a Case Of Childhood Hypophosphatasia

, 2019
Ghufran Babar
openalex   +1 more source

PHOSPHO1 is Essential for Normal Bone Fracture Healing [PDF]

, 2018
Al-Jallad , Hadil, Farquharson, Colin, Hamdy, Reggie, Li, Jingjing, millan, jose luis, Morcos, Mina, Murshed, Monzur   +6 more
core   +1 more source

Adult Hypophosphatasia in a Middle-Aged Patient With Recurrent Fractures: Prevention of New Fractures With Asfotase Alfa. [PDF]

JCEM Case Rep
Inoue R, Ishizawa K, Takamura Y, Kosokabe F, Takeuchi K, Inoue D.   +5 more
europepmc   +1 more source

Glycosylation‐deficient mutations in tissue‐nonspecific alkaline phosphatase impair its structure and function and are linked to infantile hypophosphatasia [PDF]

, 2016
Keiichi Komaru, Yasuhito Satou, Hiba A. Al‐Shawafi, Natsuko Numa‐Kinjoh, Miwa Sohda, Kimimitsu Oda   +5 more
openalex   +1 more source