Results 201 to 210 of about 1,672 (232)

Exploring MAPT-containing H1 and H2 haplotypes in Parkinson’s disease across diverse populations

Reyes-Pérez P, Hor JW, Toh TS, Sanyaolu AO, Pantazis CB, Leal TP, Yeboah S, Bandres-Ciga S, Morris HR, Makarious MB, Senkevich K, the Latin American Research Consortium on the Genetics of Parkinson’s Disease (LARGE-PD), the Global Parkinson’s Genetics Program (GP2), Leonard H, Brolin KA.   +14 more
europepmc   +1 more source

The three stages of religious decline around the world. [PDF]

Nat Commun
Stolz J, de Graaf ND, Hackett C, Antonietti JP.   +3 more
europepmc   +1 more source

‘reportless places’: Janet Malcolm and Collage

Critical Quarterly, EarlyView.
Natalie Ferris
wiley   +1 more source

Two Faces of the Anti‐Inclusion Neoconservative Coin in Brazil: Neoliberalism and Far‐Right

Gender, Work &Organization, EarlyView.
ABSTRACT Brazil has recently experienced the resurgence of the far‐right, a movement that has also occurred in other countries around the world. Given this context, this article seeks to understand the factors that enabled the union among neoliberalism, neoconservatism, and the far‐right in Brazil, demonstrating that in times of economic crisis the ...
Eloisio Moulin de Souza
wiley   +1 more source

Fritz Kauffmann: innovator in microbial classification. [PDF]

APMIS
Jønsson R, Ingholt MM, Krogfelt KA.
europepmc   +1 more source

Rare Bleeding Disorders and Bleeding Disorder of Unknown Cause: Current Understanding and Recent Developments

Haemophilia, EarlyView.
ABSTRACT Rare bleeding disorders (RBDs) represent a diverse group of inherited conditions involving coagulation factors or platelets. These conditions, such as Glanzmann thrombasthenia (GT) or severe coagulation factor deficiencies, are uncommon. In contrast, bleeding disorder of unknown cause (BDUC) is a diagnosis of exclusion without an identifiable ...
Alessandro Casini, Robert Klamroth, Bauke Haisma, Dino Mehic, Saskia E. M. Schols   +4 more
wiley   +1 more source

APF2: an improved ensemble method for pharmacogenomic variant effect prediction. [PDF]

Pharmacogenomics J
Zhou Y, Pirmann S, Lauschke VM.
europepmc   +1 more source

Perioperative Outcomes in Factor XI Deficiency: A Systematic Review

Haemophilia, EarlyView.
ABSTRACT Background Congenital factor XI (FXI) deficiency has a variable bleeding phenotype, and FXI activity alone does not predict perioperative bleeding. Management practices remain heterogeneous, and available evidence derives from case reports, small case series, and retrospective cohorts.
Zainab Al‐Housni, Raeesah Mohammed, Silvio Ligia, Jim Douketis, Chatree Chai‐Adisaksopha, Alfonso Iorio, Davide Matino   +6 more
wiley   +1 more source

Preconception Care and Genetic Screening: A Global Review and Strategic Perspectives for Implementation in Bulgaria. [PDF]

Children (Basel)
Hristova-Atanasova E, Micallef M, Stivala J, Iskrov G, Gyokova E.   +4 more
europepmc   +1 more source

Guises of Despair

European Journal of Philosophy, EarlyView.
Béatrice Han‐Pile
wiley   +1 more source