Showing results (691-700 of 4,757) with videos related to

Sort By:
Pageof 476
Orphanet Journal of Rare Diseases|June 29, 2023
Physician- and patient-reported perspectives on myasthenia gravis in Europe: a real-world surveyMilada Mahic, Ali Bozorg, Jonathan DeCourcy, et al.
Orphanet Journal of Rare Diseases|June 18, 2023
SCARB1 downregulation in adrenal insufficiency with Allgrove syndromeGiacomo Bitetto, Gianluca Lopez, Dario Ronchi, et al.
Orphanet Journal of Rare Diseases|June 26, 2023
Pituitary abscess: a case report and systematic review of 488 casesFelicity Stringer, Yi Chao Foong, Alanna Tan, et al.
Orphanet Journal of Rare Diseases|January 5, 2019
Achondroplasia: a comprehensive clinical reviewRichard M Pauli
Orphanet Journal of Rare Diseases|February 1, 2019
Incidental screen positive findings in a prospective cohort study in Matlab, Bangladesh: insights into expanded newborn screening for low-resource settingsMalia S Q Murphy, Pranesh Chakraborty, Jesmin Pervin, et al.
Orphanet Journal of Rare Diseases|September 7, 2020
The TAND checklist: a useful screening tool in children with tuberous sclerosis and neurofibromatosis type 1Francesca Cervi, Veronica Saletti, Katherine Turner, et al.
Orphanet Journal of Rare Diseases|March 19, 2020
Abnormally increased carotid intima media-thickness and elasticity in patients with Morquio A diseaseRaymond Y Wang, Kyle D Rudser, Donald R Dengel, et al.
Orphanet Journal of Rare Diseases|September 10, 2020
Further evidence for POMK as candidate gene for WWS with meningoencephaloceleLuisa Paul, Katrin Rupprich, Adela Della Marina, et al.
Orphanet Journal of Rare Diseases|September 15, 2020
Distal muscle weakness is a common and early feature in long-term enzyme-treated classic infantile Pompe patientsJ J A van den Dorpel, E Poelman, L Harlaar, et al.
Orphanet Journal of Rare Diseases|September 12, 2020
Grisel's syndrome in Kawasaki diseaseXiaoliang Liu, Kaiyu Zhou, Yimin Hua, et al.
Pageof 476