Results 31 to 40 of about 1,880 (148)
The Concise Guide to PHARMACOLOGY 2025/26: Transporters
British Journal of Pharmacology, Volume 182, Issue S1, Page S404-S496, December 2025.The Concise Guide to Pharmacology 2025/26 marks the seventh edition in this series of biennial publications in the British Journal of Pharmacology. Presented in landscape format, the guide provides a comparative overview of the pharmacology of drug target families. The concise nature of the Concise Guide refers to the style of presentation, being clear,
Stephen P. H. Alexander +28 more
wiley +1 more source
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement [PDF]
, 2018 This Consensus Statement covers recommendations for the diagnosis and management of patients with pseudohypoparathyroidism (PHP) and related disorders, which comprise metabolic disorders characterized by physical findings that variably include short ...
Ahmed, S.F. (Sayed) +45 more
core +2 more sources
Archivos Argentinos de PediatriaHere we describe the case of a 2-month-old infant who consulted several times due to excessive crying, initially interpreted as having a gastrointestinal cause. Since the symptom persisted, a fracture was suspected due to its association with mobilization of the limbs and palpation of a mass on the anterior aspect of the right tibia.
Ana, Braslavsky, María E, López
openaire +2 more sources
Un caso de betatalasemia en un niño de una necrópolis tebana del Imperio Nuevo. La etiopatogenia de la cribra orbitalia a revisión [PDF]
, 2011 X Congreso Nacional de Paleopatología.
Baxarias, J. +4 more
core
Caffey disease – A rare case report. [PDF]
, 2023 8 month old male infant with localized swelling of the thigh, fever and ...
Das, Dr Sudha Kiran
core +1 more source
Mimics and Pitfalls of Imaging Assessment [PDF]
, 2021 Axial spondyloarthritis (axSpA) is a chronic inflammatory disorder that predominantly involves the axial skeleton. Imaging findings of axSpA can be divided into active changes, which include bone marrow edema, synovitis, enthesitis, capsulitis, and intra-
Caetano, António Proença +2 more
core +3 more sources
Prenatal Diagnosis of Proteus Syndrome: About a Case
American Journal of Medical Genetics Part A, Volume 197, Issue 5, May 2025.ABSTRACT Proteus syndrome (PS) is a rare disorder (< 1/1000000), marked by progressive overgrowth commonly impacting the skeleton, skin, adipose tissue, and central nervous system. Clinical criteria were established in 2019. PS arises from a somatic activating variation in the AKT1 gene.
Luana Giovannangeli +10 more
wiley +1 more source
Health Science Reports, Volume 8, Issue 5, May 2025.ABSTRACT Background and Aims Children with congenital heart disease (CHD) often require complex pharmacotherapy for symptom management and complication prevention. However, their unique physiological profiles increase vulnerability to drug‐related side effects.
Esmaeel Toni +3 more
wiley +1 more source
Managing the patient with osteogenesis imperfecta: a multidisciplinary approach [PDF]
, 2017 Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized by low bone density. The type and severity of OI are variable.
Bishop, N., Marr, C., Seasman, A.
core +1 more source
Glycerophospholipids: Roles in Cell Trafficking and Associated Inborn Errors
Journal of Inherited Metabolic Disease, Volume 48, Issue 2, March 2025.ABSTRACT Glycerophospholipids (GPLs) are the main lipid components of cellular membranes. They are implicated in membrane structure, vesicle trafficking, neurotransmission, and cell signalling. GPL molecules are amphiphilic, organized around the three carbons of glycerol. Positions sn‐1 and sn‐2 are each esterified to a fatty acid (FA).
Foudil Lamari +2 more
wiley +1 more source