Results 211 to 220 of about 591,971 (351)

Comparative gender biases in models of personality disorder [PDF]

, 2009
Douglas B. Samuel, Thomas A. Widiger
openalex   +1 more source

Factor XIII Supplementation in Postpartum Hemorrhage: From Biological Rationale to Clinical Implementation

American Journal of Hematology, EarlyView.
ABSTRACT Postpartum hemorrhage (PPH) remains the leading cause of preventable maternal mortality despite standard interventions. Recent fibrinogen trials failed to improve outcomes, prompting interest in coagulation factor XIII (FXIII). FXIII functions as “molecular cement,” cross‐linking fibrin and stabilizing clots.
Jeremy W. Jacobs, Elizabeth A. Abels, Brian D. Adkins, Garrett S. Booth, Victoria Costa, Sheharyar Raza, Michelle Simon, Jennifer S. Woo, Allison P. Wheeler   +8 more
wiley   +1 more source

Role of Early Trauma on Defense Mechanisms and Coping Strategies in Personality Disorders. [PDF]

Medicina (Kaunas)
Turiaco F, Iannuzzo F, Lombardo C, Clementi V, Mento C, Drago A, Bruno A, Muscatello MRA, Pandolfo G.   +8 more
europepmc   +1 more source

Recidivism and mental illness: Correctional strategies to reduce recidivism in offenders with attention deficit hyperactivity and borderline personality disorders

, 2020
Courtney J. Eddy
openalex   +1 more source

General hospital admission rates in people diagnosed with personality disorder

, 2019
Marcella Fok, Chin‐Kuo Chang, Mathew Broadbent, Robert Stewart, Paul Moran   +4 more
openalex   +2 more sources

Autosomal Dominant Erythrocytosis Caused by Non‐Renal Erythropoietin (EPO) Due to EPO c.‐136 G>A Germline Mutation

American Journal of Hematology, EarlyView.
A novel erythropoietin (EPO) promoter mutation (c.‐136 G>A) causes autosomal dominant erythrocytosis via non‐renal expression of EPO. ABSTRACT We previously reported a five‐generation kindred with autosomal dominant erythrocytosis associated with a novel germline promoter variant in the erythropoietin (EPO) gene (EPO c.‐136 G>A).
Lucie Lanikova, Dusan Hrckulak, Veronika Zimolova, Felipe R. Lorenzo, Jihyun Song, Katerina Vecerkova, Olga Babosova, Linda Berkova, Vladimir Korinek, Steve Elliott, Josef T. Prchal   +10 more
wiley   +1 more source

Editorial: Reviews in psychiatry 2023: personality disorders. [PDF]

Front Psychiatry
Beghi M, Sanza M.
europepmc   +1 more source

Psychotherapists’ emotional and physiological reactions toward patients with either borderline personality disorder or depression

, 2019
Natalia Putrino, Leandro Martín Casari, Belén Mesurado, Martín Etchevers   +3 more
openalex   +2 more sources

GATA3 Deletion Associated With Juvenile Idiopathic Arthritis: Expanding the Phenotypic Spectrum of Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss, Amanda V. Karam, Julia Shalen, David E. Tunkel, Belina Y. Yi, Kelsey S. Guthrie, Emily M. Kudalkar, Anna E. Patrick, Sonja A. Rasmussen   +8 more
wiley   +1 more source

Developing loneliness interventions for people with personality disorders: A call to action. [PDF]

Ann N Y Acad Sci
Reinhard MA, Padberg F.
europepmc   +1 more source