Results 31 to 40 of about 5,729,296 (288)
Psychiatry and Clinical Psychopharmacology, 2021 The term "m ood stabilizer" defines the type of a drug, w hich can be used both in cross-sectional treatm ent and in prevention, and, m ain problem atic is the polarity of the disorder besides the polarity in the treatm ent.
Timuçin ORAL
doaj
Pediatric Blood &Cancer, EarlyView.ABSTRACT Purpose Although not always achieved, complete chemotherapy‐induced nausea and vomiting (CINV) control is the conventional goal of CINV prophylaxis. In this two‐center, mixed‐methods study, we sought to understand the preferences of adolescent patients and family caregivers for CINV control endpoints.
Haley Newman +8 more
wiley +1 more source
Intravitreal GD2‐Specific Chimeric Antigen Receptor T‐Cell Therapy for Refractory Retinoblastoma
Pediatric Blood &Cancer, EarlyView.ABSTRACT Effective treatments for advanced, treatment‐resistant retinoblastoma (RB) remain limited. GD2‐specific chimeric antigen receptor (CAR) T cells show potent antitumor activity with minimal toxicity but have not previously been evaluated in RB.
Subongkoch Subhadhirasakul +13 more
wiley +1 more source
Selefin ve Halefin Tevil Yaklaşımları ve Bunun Tefsire Yansımaları
Antakiyat, 2022 Kavramlara yüklenen anlamlar, onlara yönelik yaklaşımların belirlenmesinde büyük bir öneme sahiptir. Dolayısıyla muhatabın bir kavram ile ilgili algısının mahiyetini doğru bir şekilde anlayabilmek için onun o kavrama yüklediği anlamları bilmek gerekir ...
Murat Oral
doaj
Pediatric Blood &Cancer, EarlyView.ABSTRACT Background Kaposiform lymphangiomatosis (KLA) is an aggressive complex lymphatic anomaly. Patients exhibit malformed lymphatic vessels and often develop hemorrhagic effusions and elevated angiopoietin‐2 (Ang‐2) levels. A somatic NRAS p.Q61R (NRASQ61R) mutation has been associated with KLA.
C. Griffin McDaniel +3 more
wiley +1 more source
Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report
Pediatric Blood &Cancer, EarlyView.ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan +6 more
wiley +1 more source
Variable Temperature-Scanning Hall Probe Microscopy (VT-SHPM) with GaN/AlGaN Two-Dimensional Electron Gas (2DEG) Micro Hall Sensors in 4.2-425K range, Using Novel Quartz Tuning Fork AFM Feedback [PDF]
, 2008 In this report, we present the fabrication and variable temperature (VT) operation of Hall sensors, based on GaN/AlGaN heterostructure with a two-dimensional electron gas (2DEG) as an active layer, integrated with Quartz Tuning Fork (QTF) in atomic ...
Oral, Ahmet
core
Pediatric Blood &Cancer, EarlyView.ABSTRACT Background Osteosarcoma (OS) and Ewing sarcoma (EWS) are the most common primary bone cancers in children, but acute thrombosis is poorly characterized in this population. Our study evaluated the rates of venous thromboembolism (VTE) and associated risk factors in pediatric patients with bone sarcomas treated over a 10‐year period encompassing
Sarah Kappa +8 more
wiley +1 more source
GAZÂLÎ’DE HABERÎ SIFAT VE TE’VİL METODOLOJİSİ
Akademik İncelemeler Dergisi, 2019 Haberî sıfatlar,el, parmak, yüz ve kadem gibi nasslarda geçen ancak aklî deliller nedeniylezâhirî mânâlarıyla; nasslar içindeki bağlamları yani siyâk, sibâk ve sevkdışında, tek başına Allah’a nispet edilemeyen sıfatlardır.
Osman Oral
doaj +1 more source
HABİB EN-NECCAR’IN ANTAKYA HALKINA TAVSİYE ETTİĞİ PSİKOSOSYAL HİKMETLER
Mehmet Akif Ersoy Üniversitesi Sosyal Bilimler Enstitüsü Dergisi, 2020 Habîb en-Neccâr, Hz. İsa’nın peygamberliği döneminde Antakya’da yaşadığı tahmin edilen biridir. O dönemde bir şehir halkına tevhid dinini tebliğ etmeleri için Allah (veya Hz. İsa) elçilerini gönderir.
Osman Oral
doaj +1 more source