Results 241 to 250 of about 45,743 (302)

Osteomyelitis of the lumbar vertebrae.

Minnesota medicine, 2010
openaire   +1 more source

Spectrum of Hypogonadism and Its Management in Adolescents With Prader‐Willi Syndrome: A Retrospective Cohort Study Over 35 Years

Clinical Endocrinology, Volume 105, Issue 1, Page 51-59, July 2026.
ABSTRACT Context Adult data indicate that hypogonadism is underdiagnosed and undertreated in Prader‐Willi Syndrome (PWS). Objectives We aimed to describe the spectrum of pubertal development, and the diagnosis and treatment of hypogonadism in paediatric/adolescent patients with PWS. Design/Patients A retrospective cohort study of patients with PWS aged
Helen Nguyen, Geoffrey Ambler, Yoon Hi Cho   +2 more
wiley   +1 more source

Entering a new era for exercise countermeasures in human spaceflight

Experimental Physiology, EarlyView.
Enrico De Martino, Patrick Swain, Kirsty Lindsay, Claire Bruce‐Martin, Ewoud Jacobs, Bradley Barbour, Chris Buckley, Adam C. McDonnell, Nick Caplan, Luke Hughes   +9 more
wiley   +1 more source

Variation in trabecular bone microarchitecture across rhesus macaque (Macaca mulatta) load‐bearing joints

Journal of Anatomy, Volume 249, Issue 1, Page 97-113, July 2026.
Aging of bone density (BV/TV) is regional: Forelimb [left] elements gain bone sporadically (orange) but hind limb elements [right] lose bone globally (blue). Abstract Globally, human population structure is quickly trending older, increasing the prevalence and systemic burden of age‐related skeletal disorders such as osteoporosis.
Cassandra M. Turcotte, Aditi Raghunath, Timothy M. Ryan, Lily J. D. DeMars, Erin Siracusa, Sam K. Patterson, Cayo Biobank Research Unit, Michael L. Platt, Lauren J. N. Brent, Noah Snyder‐Mackler, Samuel E. Bauman, Michael J. Montague, Melween I. Martinez, Scott A. Williams, Susan C. Antón, James P. Higham, Sharon Kuo   +16 more
wiley   +1 more source

The junction between the midgut and hindgut co‐localizes with the rectosigmoid junction

Journal of Anatomy, Volume 249, Issue 1, Page 33-53, July 2026.
At 5 weeks of development, the midgut has formed its primary loop (left). It is well established that the midgut is bounded cranially by the caudal end of the ventral mesentery and the presence of the common bile duct, but its caudal boundary remains to be established.
Hui Gao, Nutmethee Kruepunga, Greet Mommen, Susanne E. Köhler, Jill P. J. M. Hikspoors, Wouter H. Lamers   +5 more
wiley   +1 more source

Fused lumbar vertebrae

, 2015
openaire   +1 more source

Significance of fiber orientation in the interosseous sacroiliac ligament: An anatomical and histological study of the implications of its mechanical adaptation

Journal of Anatomy, Volume 249, Issue 1, Page 68-77, July 2026.
Fiber structure of the interosseous sacroiliac ligament exhibits a distinct organization, with predominantly vertical fibers in the inferior region and predominantly horizontal fibers in the superior region. These fiber alignment patterns likely reflect mechanical adaptation to the sacroiliac joint motion and may support imaging‐based evaluation of its
Masahiro Tsutsumi, Akimoto Nimura, Hajime Utsunomiya, Takuya Ibara, Shintarou Kudo, Keiichi Akita   +5 more
wiley   +1 more source

Magnetic Resonance Imaging Features of Intravascular Osteosarcoma Affecting the Ventral Internal Vertebral Venous Plexus Causing Cervical Myelopathy in a Dog

Veterinary Radiology &Ultrasound, Volume 67, Issue 4, July 2026.
ABSTRACT A 10.5‐year‐old male castrated Standard Poodle was referred for the evaluation of chronic C6–T2 myelopathy. MRI revealed a severe asymmetric enlargement of the ventral internal vertebral venous plexus, intervertebral/vertebral veins, and possibly the C6 basivertebral vein, with secondary mild spinal cord compression.
Robert Wise, Rachel Durrwachter, Nathan Fanzone, Wilfried Mai   +3 more
wiley   +1 more source

Homozygous Achondroplasia With Long‐Term Survival: Growth Patterns, Medical Interventions, and Practice Implications

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1372-1377, June 2026.
ABSTRACT Homozygous achondroplasia is widely considered perinatal lethal by the medical community. In this case series, we report two children from a single family with longer‐term survival. One child lived for 17 months and the other was 60 months at the time of publication.
Hannah Singerline, Jason Laufman, Kimberly Wallis, Michelle Merrill   +3 more
wiley   +1 more source

Expanding the Evaluation of Skeletal Anomalies in Patients With KBG Syndrome: Recommendations for Clinical Practice

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1306-1314, June 2026.
ABSTRACT KBG syndrome is a rare autosomal dominant neurodevelopmental disorder caused by ANKRD11 haploinsufficiency and is characterized by short stature, distinctive facial features, intellectual disability or developmental delay, congenital anomalies and skeletal anomalies.
Marit van der Leij, Emilie de Groot, Eleonora Orlandini, Willemijn M. Klein, Charlotte W. Ockeloen, Joyce M. Geelen   +5 more
wiley   +1 more source