Results 111 to 120 of about 1,619,649 (263)

The Global Theranostics Access Gap: Real-World Disparities in PSMA PET/CT and ¹⁷⁷Lu-PSMA Therapy Between Centers in Brazil and Europe. [PDF]

J Nucl Med
Cerci JJ, Fanti S, Herrmann K, Rodrigues DF, Leite PHF, Masukawa M, da Silva MM, Fendler WP, Goncalves E Silva A, Sanfelice EN, Ayelet W, Ghetti F, Bascioni A, Estrado Lobato EE, Paez D.   +14 more
europepmc   +1 more source

Preferential trading in agriculture: New insights from a structural gravity analysis and machine learning

American Journal of Agricultural Economics, EarlyView.
Abstract Preferential trade agreements (PTAs) contain various non‐tariff provisions, yet identifying their trade effects remains challenging because these commitments are high‐dimensional and strongly correlated within agreements. We estimated a theory‐consistent structural gravity model with domestic flows for 26 agricultural subsectors over 1988–2017
Dongin Kim, Sandro Steinbach
wiley   +1 more source

Transmission Dynamics of Dengue Virus, Ceará State, Brazil, 2010-2025. [PDF]

Emerg Infect Dis
de Lima STS, Claro IM, Hua X, Sacchetto L, de Jesus R, Simões Mello LM, Forato J, Manuli ER, McDonald C, de Lima MET, Ferraz CPM, Duarte LMF, Viana VAF, Costa MA, Firmino AC, Abrantes JJPA, Sena LOC, Silva DB, Macedo SMS, Sabino EC, do Carmo RF, Croda J, Proenca-Modena JL, de Souza WM.   +23 more
europepmc   +1 more source

A mid‐Cretaceous monocot flower from the Dakota Sandstone of Kansas and its potential implications for the fossil record of palms

American Journal of Botany, EarlyView.
Abstract Premise Although the megafossil flora of the upper Albian–lower Cenomanian Dakota Formation in Kansas is well known for angiosperms, monocots have not been reported previously. Methods A mesofossil flower was discovered by X‐ray analysis of a specimen collected more than a century ago from the Dakota Sandstone of central Kansas.
Bruce H. Tiffney, Walter S. Judd, William J. Baker, John Dransfield, Steven R. Manchester   +4 more
wiley   +1 more source

New Record of Raillietiella furcocerca (Pentastomida: Raillietiellidae) in Bothrops atrox from the Brazilian Amazon: Morphological Characterization and Infection Sites. [PDF]

Acta Parasitol
Sarmento ACO, Chagas-de-Souza D, Bassini-Silva R, Alves-Coêlho T, Ribeiro S, Corrêa LL, Santos-Jr AP.   +6 more
europepmc   +1 more source

First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%–5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature.
Gabriela Roldão Correia‐Costa, Joana Rosa Marques Prota, Antonia Paula Marques‐de‐Faria, Carlos Eduardo Steiner, Társis Paiva Vieira   +4 more
wiley   +1 more source

Epidemiological trajectory of Mpox in Brazil, 2022-2025: evidence of geographic consolidation and syndemic burden. [PDF]

R Soc Open Sci
Soares GDN, Innocente-Alves C, Marques AL, da Silva Dal Pizzol T, Campos FS, Santi L, Beys-da-Silva WO.   +6 more
europepmc   +1 more source

Differential Diagnosis of Mucopolysaccharidoses Types I, II, III, IVA, and VI Through Analysis of Leukocytic Inclusions

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Mucopolysaccharidoses (MPS) are lysosomal storage disorders characterized by the accumulation of glycosaminoglycans (GAGs), which can lead to cytoplasmic alterations in leukocytes. The objective of this study was to characterize leukocyte inclusions in patients with different types of MPS and assess their diagnostic relevance.
Márcio A. W. Melo, Marcelo S. Kertenetzky, Cristina M. Silveira, Maíra M. Ribeiro, Paula F. Medeiros, Gabriela S. Arcanjo   +5 more
wiley   +1 more source

Repply to: When technology advances faster than competence: the risk of deskilling in obstetrics and gynecology. [PDF]

Rev Bras Ginecol Obstet
da Silva AL, Cordioli E, Podgaec S, de Sá MFS, Wender MCO.   +4 more
europepmc   +1 more source

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Van Maldergem syndrome (VMLDS) is an ultra‐rare autosomal recessive disorder characterized by craniofacial dysmorphism, intellectual disability, hypotonia, skeletal anomalies, and feeding difficulties. It is caused by biallelic variants in DCHS1 or FAT4 genes.
Gabriela Roldão Correia‐Costa, Bruna Fagundes Rodrigues Alaite, Vera Lúcia Gil‐da‐Silva‐Lopes, Carlos Eduardo Steiner, Társis Paiva Vieira   +4 more
wiley   +1 more source