Results 251 to 260 of about 508,254 (320)

Single-Stage Treatment of a Patellar Osteochondral Defect in an Adolescent Using Autologous Minced Cartilage - Platelet-Rich Plasma Scaffold Technique: A Case Report and Technical Considerations. [PDF]

J Orthop Case Rep
Rajendrababu AR, Prasad A, Nazar RT, Mathew RJ, John JT, Menon P.   +5 more
europepmc   +1 more source

MTCA‐Net: Multi‐Task Cascade Analysis Network for Real‐Time Sperm Quality Analysis

Advanced Intelligent Systems, EarlyView.
This article proposes MTCA‐Net, a multi‐task cascaded analysis network for real‐time sperm quality assessment in intracytoplasmic sperm injection. The framework integrates detection, tracking, and segmentation modules to jointly analyze sperm morphology and motility.
Jiajin Li, Wenwen Sun, Jun He, Xinyu Fan, Xuecheng Ge, Fengya Lu, Yadan Wang, Yi Wang, Zhiguo Zhang, Qibing Wu, Jinhua Zhou   +10 more
wiley   +1 more source

What are the Chances of MACI Approval in the United States? A Deep Dive into the Insurance Authorization Data. [PDF]

Cartilage
Cavendish PA, Milliron EM, Peterson CJ, Sherman SL, Jones DG, Strauss EJ, Flanigan DC.   +6 more
europepmc   +1 more source

Relative Exchangeable Copper Confirms Wilson Disease and Supports Reclassification of the ATP7B p.Met665Ile Variant With Conflicting Pathogenicity Evidence

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Wilson disease (WD) is an autosomal recessive disorder of copper metabolism caused by ATP7B mutations. Diagnosis is usually straightforward in symptomatic patients, but can be challenging in children and adolescents with mild liver disease, borderline urinary copper excretion, or inconclusive genetic findings.
Emanuele Nicastro, Caterina Zuccoli, Roberto Marozzi, Antonino Barletta, Lisa Licini, Paola Tebaldi, Valeria Casotti, Mariangela Stinco, Lidia Pezzani, Maria Iascone, Lorenzo D'Antiga   +10 more
wiley   +1 more source

VACTERL association: a case report highlighting multisystem anomalies and the critical need for multidisciplinary care in Palestine. [PDF]

Int J Surg Case Rep
Milhem MI, Al-Junaidi SZ, Jabareen AE, Housheya MZ, Khamayseh WM, Milhem MI.   +5 more
europepmc   +1 more source

Optimizing Diagnostic Accuracy of Clinical Red Flags in RASopathies

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT RASopathies are a group of genetic disorders caused by pathogenic variants in the RAS‐mitogen‐activated protein kinase (RAS–MAPK) signaling pathway, often presenting with congenital heart defects, craniofacial dysmorphisms, and developmental delays. To assess the diagnostic yield of genetic testing in patients with suspected RASopathies and to
Emanuele Bobbio, Martina Caiazza, Emanuele Monda, Giustina Aruta, Alberto Budillon, Augusto Esposito, Adelaide Fusco, Annapaola Cirillo, Marta Rubino, Immacolata Viscovo, Gioacchino Scarano, Matteo Della Monica, Vincenzo Nigro, Giulio Piluso, Leandro Pecchia, Maria Giovanna Russo, Giuseppe Limongelli   +16 more
wiley   +1 more source

How I do it: exoscopic minimally invasive pericranial flap harvest for endoscopic anterior skull base reconstruction. [PDF]

Acta Neurochir (Wien)
Wiedmann MKH, Steineger JE, Dahlberg D, Dheyauldeen S.   +3 more
europepmc   +1 more source

Interim Maxillary Obturator Rehabilitation of an Aramany Class II Defect Following Resection for Oral Squamous Cell Carcinoma: A Case Report. [PDF]

J Pharm Bioallied Sci
Sonkesriya S, Pugang T, Gupta A, Soni M, Maheshwari A, Shaikh S.   +5 more
europepmc   +1 more source

Surgical management of ventricular septal rupture post device migration: a case report. [PDF]

J Cardiothorac Surg
Jaswal V, Edem S, Mishra AK, Kheni A, Reddy L.   +4 more
europepmc   +1 more source