Results 121 to 130 of about 13,529 (354)
ABSTRACT Talquetamab is a GPRC5D × CD3 bispecific antibody approved for relapsed/refractory multiple myeloma (RRMM). This is the first real‐world study to comprehensively report muco‐cutaneous toxicities, infections, and efficacy of talquetamab in 151 patients across five countries with the longest follow‐up reported enabling better efficacy and ...
Murali Janakiram +94 more
wiley +1 more source
The Eastern Palace of Qatna and the Middle Bronze Age Architectural Tradition of Western Syria
Although Qatna has been the object of systematic archaeological investigations since 1999 (leaving aside the campaigns of the French Mission under the direction of Robert du Mesnil du Buisson) and although it is, together with Mari, Aleppo and ...
IAMONI, Marco
core
Author Correction: A Tunguska sized airburst destroyed Tall el-Hammam a Middle Bronze Age city in the Jordan Valley near the Dead Sea. [PDF]
Bunch TE +20 more
europepmc +1 more source
ABSTRACT Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) is an autosomal recessive mitochondrial defect of long‐chain fatty acid β‐oxidation, caused by biallelic pathogenic variants in HADHA or HADHB. We report a 22‐year‐old male with an atypically mild presentation of LCHADD who was referred to the Undiagnosed Diseases Network (UDN ...
Yutaka Furuta +9 more
wiley +1 more source
New relative sea-level (RSL) indications from the Eastern Mediterranean: Middle Bronze Age to the Roman period (~3800-1800 y BP) archaeological constructions at Dor, the Carmel coast, Israel. [PDF]
Yasur-Landau A +9 more
europepmc +1 more source
Transformations in the Carpathian Basin around 1600 B. C.
Um die Zeit des Vulkanausbruchs von Thera fanden wichtige Veränderungen im Karpatenbecken statt. Diese sogenannte Koszider Epoche korrespondiert mit der letzten Phase der mittleren Bronzezeit in der ungarischen Terminologie und stellt den Übergang ...
Kulcsár, Gabriella +3 more
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ABSTRACT Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) is an autosomal recessive inborn error of metabolism caused by biallelic pathogenic variants in one of three known genes: ETFA, ETFB, and ETFDH. It can cause multisystem dysfunction, including cardiomyopathy in severe cases.
Yutaka Furuta +17 more
wiley +1 more source
Defining Features of Gabriele‐de Vries Syndrome in Adults: A Case Report and Literature Review
ABSTRACT Gabriele‐de Vries syndrome (GADEVS) is a neurodevelopmental disorder caused by heterozygous pathogenic variants in the YY1 gene. Like most rare genetic syndromes, the adult manifestations of GADEVS remain poorly defined. Here, we describe the oldest patient reported to date with GADEVS—a 63‐year‐old woman with a c.1177_1179del YY1 variant ...
Ethan W. Hollingsworth, Changrui Xiao
wiley +1 more source
Social Variation in Middle Bronze Age Knossos
The present study uses high-quality data on stable carbon (13C/12C) and nitrogen (15N/14N) isotope ratio from two Middle Bronze Age human skeletal collections from Knossos for the purposes of a palaeodietary investigation in this context, and offers a ...
Nafplioti, Argyro
core +1 more source
Beycesultan: v. 2 Middle Bronze age architecture and pottery [PDF]
v. 1, 3, pt. 1 : ill. ; 28 cm. | v. 1. The Chalcolithic and early Bronze age levels.--v. 2. Middle Bronze age architecture and pottery.--v. 3., pt. 1.
Mellaart, James
core

