Gender Differences Among Urologists in the Assessment and Utilization of ESWL Treatment: Insights from a Multinational Survey of 3747 Participants. [PDF]
J Clin MedKarim H +14 more
europepmc +1 more source
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago
Movement Disorders, EarlyView.Abstract Background SLC7A6OS c.191A>G is a rare, autosomal recessive cause of progressive myoclonus epilepsy (PME). The c.191A>G variant, first discovered in two families from Türkiye and Portugal, was recently identified in three additional probands from the USA, all of Puerto Rican ancestry.
Bronwyn E. Grinton +17 more
wiley +1 more source
Celiac disease and developmental delay as the first manifestations of tripeptidyl peptidase 2 deficiency. [PDF]
Pediatr Allergy ImmunolAtes NK +11 more
europepmc +1 more source
Retraction Note: A randomized prospective comparison of the needleless mini-sling "hammock" and "U-shape" configurations for management of stress urinary incontinence: 60-month follow-up results. [PDF]
Arch Gynecol ObstetDoğan O, Başbuğ A, Eren E, Yassa M.
europepmc +1 more source
Association of Pretreatment ANR and IronMLR With Pathological Response Following Neoadjuvant Chemotherapy in Breast Cancer. [PDF]
Breast Cancer (Dove Med Press)Özge E +7 more
europepmc +1 more source
Insight into Essential and Complex Autism Spectrum Disorders: Clinical Characteristics, Chromosomal Microarray Analysis, and Risk Factors. [PDF]
Genes (Basel)Tüysüz B +8 more
europepmc +1 more source