Results 81 to 90 of about 704,033 (216)

Una nueva etapa para Advances in Laboratory Medicine/Avances en Medicina de Laboratorio

open access: yesAdvances in Laboratory Medicine, 2023
González Álvaro   +4 more
doaj   +1 more source

بررسی و معرفی انواع مطالعات سنتزی/ ترکیبی/ مروری در تحقیقات پزشکی [PDF]

open access: yesمجله دانشگاه علوم پزشکی سبزوار, 2017
اهداف: مطالعات سنتزپژوهی، راهی برای بازیابی، مرور، ترکیب، تحلیل و یکپارچه‌کردن نتایج مطالعات اصیل است. مطالعة حاضر به‌معرفی انواع روش‌های این نوع مطالعات می‌پردازد. سپس، وضعیت مقالات منتشرشده در PubMed بررسی شده است.
سمیه نادی راوندی
doaj  

Navigating Asparaginase Treatment for Patients With Acute Lymphoblastic Leukemia: US Consensus Panel Recommendations on the Role of Multidisciplinary Care

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Asparaginase is a critical treatment component for patients with acute lymphoblastic leukemia/lymphoblastic lymphoma (ALL/LBL). However, the successful delivery of asparaginase‐based therapy remains challenging across care settings due to its complex administration, distinct toxicity profile, prolonged treatment duration, and the need for ...
Amir Ali   +8 more
wiley   +1 more source

A Review on Current Challenges and Knowledge Gaps in Artificial Stone Silicosis

open access: yesAmerican Journal of Industrial Medicine, EarlyView.
ABSTRACT Background The global emergence of artificial stone (AS) silicosis represents a critical occupational health challenge. The aim of this systematic review is to provide an overview of the clinical, functional, radiological, and occupational characteristics of patients affected by AS silicosis at the time of diagnosis, and to identify current ...
Paola Mason   +8 more
wiley   +1 more source

A Novel NR3C1 Frameshift Variant Associated With Familial Glucocorticoid Resistance Syndrome: An Integrated Analysis of Steroid Profiling and Structural Modeling

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Glucocorticoid resistance syndrome (GRS) is a rare hereditary disorder caused by pathogenic variants in NR3C1, characterized by marked phenotypic heterogeneity and frequent misdiagnosis as primary aldosteronism or subclinical Cushing's syndrome.
Sufang Yun   +7 more
wiley   +1 more source

Use of the associative analysis for processing of scientific publications in the field of drugs delivery systems

open access: yesТонкие химические технологии, 2010
In this paper the associative analysis of terms' co-occurrences in the abstracts of scientific articles (more than 600 thousands publications) in the field of drug delivery system was used. The associations between 2358 biologically active chemicals were
О. А. Ugolnikova   +6 more
doaj  

Severe Phenotype in an Indian Family With Progressive Pseudorheumatoid Arthropathy of Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Progressive pseudorheumatoid arthropathy of childhood (PPAC) is a rare autosomal recessive progressive condition that affects the cartilage of joints and bones. The symptoms of PPAC include stiffness of the joints, bony swelling of the toes and fingers, short stature, kyphosis, and muscle weakness.
Narinder Singh   +5 more
wiley   +1 more source

Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC‐Related Disorder

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in CLTC, which encodes the clathrin heavy chain involved in vesicle‐mediated trafficking in neurons, cause a rare neurodevelopmental disorder associated with variable severity of global developmental delay and intellectual disability and structural brain abnormalities. Although corpus callosum and white matter anomalies are
Daniel Charouf   +7 more
wiley   +1 more source

Clinical and Molecular Characterization of 46 Patients With Beckwith–Wiedemann Spectrum and Uniparental Disomy of 11p15

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Beckwith–Wiedemann spectrum (BWSp) is an overgrowth disorder characterized by its main clinical features macrosomia, macroglossia, and abdominal wall defects. BWSp is caused by (epi)genetic chromosome 11p15 alterations with approximately 20%–27% of patients exhibiting mosaic paternal uniparental disomy of chromosome 11p15 (pUPD11p15).
Saskia M. Maas   +9 more
wiley   +1 more source

A bibliometric analysis of biochemistry theses in Türkiye: comparison with global trends

open access: yesTürk Biyokimya Dergisi
This study aims to examine the trends and distribution of research areas and methodologies in biochemistry theses over time by performing a bibliometric analysis in the CoHE database and comparing them with PubMed trends.
Özdemіr Muammer   +2 more
doaj   +1 more source

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