Results 21 to 30 of about 25,393 (96)
Long‐Term Cochlear Implant Sensitivity in Patients With Far Advanced Otosclerosis
This study aimed to evaluate mid‐ and long‐term cochlear implant fitting in otosclerosis patients compared to a control group. It suggested significant tissue remodeling at the cochlear apex in otosclerosis patients, likely increasing resistance to electrical currents delivered by the implant.
Raphaële Quatre+3 more
wiley +1 more source
The 730 nm Picosecond Titanium Sapphire Laser for Treatment of Kratom‐Induced Hyperpigmentation
ABSTRACT Objectives This case series reports the use of the 730‐nm picosecond titanium‐sapphire laser in the treatment of kratom‐induced hyperpigmentation, a dermatological side effect associated with the use of Mitragyna speciosa, which remains poorly understood. Methods A series of patients with kratom‐induced hyperpigmentation were treated using the
Alanoud A. Alhadyani+2 more
wiley +1 more source
Abstract This report describes a case of refractory ionised hypercalcaemia, of 12 months duration, in an 11‐year‐old, male, neutered beagle diagnosed with metastatic histiocytic sarcoma at postmortem examination. In this case, the parathyroid hormone levels were at the lower end of the reference interval, the parathyroid hormone‐related peptide was ...
Kerry E. Rolph+5 more
wiley +1 more source
A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease
iRADIOLOGY, EarlyView.
Lin Chen, Rui Zhou
wiley +1 more source
Nearly all cases of cryptococcosis in koalas are caused by Cryptococcus gattii species complex. A rare case of meningitis due to Cryptococcus neoformans VNI/AFLP1 (abbreviated VNI) is described in a koala with nasal colonisation by both species complexes.
A Teh+6 more
wiley +1 more source
Two Ulcers on the Chin That Developed After Fever: Quiz Case
JEADV Clinical Practice, EarlyView.
Viktor Capiau+3 more
wiley +1 more source
Heterozygous germline TET2 loss‐of‐function variants associated with an ALPS‐like phenotype
Summary Germline homozygous loss‐of‐function mutations in TET2 result in significant childhood immunodeficiency that resembles autoimmune lymphoproliferative syndrome and predisposes one to lymphoma. The implications of heterozygous variants are less well understood.
Sean Harrop+13 more
wiley +1 more source
When Brown Meets White and Blue: A Quiz in Three Hues
JEADV Clinical Practice, EarlyView.
Chiara Battilotti+4 more
wiley +1 more source
EBV‐ MTX‐DLBCL shows higher driver gene mutation rates and worse outcomes after MTX discontinuation compared to EBV+ MTX‐DLBCL. IDD‐LPDs have lower mutation rates in genes related to clonal hematopoiesis (TET2/DNMT3A) and immune evasion (CD58) compared to EBV + DLBCL. ABSTRACT The WHO recently changed the outline of immunodeficiency/dysregulation (IDD)‐
Takumi Takahashi+12 more
wiley +1 more source