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Toplam kayıt 127, listelenen: 101-110
Artificial intelligence to assist better myeloma care, is it the time?
(Cıg Media Group, 2019)
Myeloma treatment made an enormous progress during the last decade. Armamentarium is grossly enlarging each year in the field of treatment. Parallel to the progress achieved to provide better care for myeloma patients, ...
The investigation of genetic etiology in familial cases with congenital hypothyroidism
(Karger, 2019)
Background: Congenital hypothyroidism(CH) is the most common neonatal endocrinological disorder in the world. Although most of the CH is sporadic, some genetic defects are responsible from the etiology. The aim of this ...
The effect of improved metabolic risk factors and metformin therapy on circulating hepatokines in obese, insulin-resistant adolescents
(Karger, 2019)
Introduction: The molecular mechanisms underlying insulin resistance (IR) is complex and has not been fully elucidated yet. The experimental studies point out the role of liver-derived proteins, called hepatokines. Aims: ...
Single carrier transmission for urllc with adaptive radio resource utilization
(Institute of Electrical and Electronics Engineers Inc., 2019)
Next generation of wireless communication systems is expected to support a wide set of applications and use cases. Among these, applications with ultra-reliable and low-latency communications (URLLC) are at utmost importance ...
Clinical relevance of minor histocompatibility antigens
(Pergamon-Elsevier Science, 2019)
Objective: The minor histocompatibility antigens (MiHA) are epitopes composed of polymorphic essential peptides evoking alloimmune responses limited to a variety of human leukocyte antigen (HLA) alleles. These peptides are ...
A rare complication of hematopoietic stem cell transplantation: Kaposi sarcoma
(Pergamon-Elsevier Science, 2019)
Background: Kaposi sarcoma is a neoplasm characterized by mucocutaneous and visceral angioproliferations that requires infection with human herpes virus (HHV)-8 for its development. The iatrogenic variant is ...
A novel homozygous nonsense mutation (p.R516X) in the SLC5A5 gene causing congenital hypothyroidism
(Nature Publishing Group, 2019)
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Evaluation of brain MRI lesions in 381 girls with central precocious puberty
(Karger, 2019)
Central precocious puberty (CPP) in girls is a diagnosis increasingly made by the Pediatric Endocrinologists worldwide. Although it is most frequently of idiopathic origin, magnetic resonance imaging (MRI) of the brain is ...
Transient gonadal activation and infant growth velocity
(Karger, 2019)
Background: Hypothalamic-pituitary-gonadal axis is activated during the first 6 months of life, called as mini-puberty in which reproductive hormone levels may reach to adult levels. Although, our understanding of the ...