Search Results - "Altuntaş, Cansu"
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Proline-stimulated signaling primarily targets the chlorophyll degradation pathway and photosynthesis associated processes to cope with short-term water deficit in maize
Published in Photosynthesis research (01-04-2020)“…Increased photosynthetic efficiencies in genotypes with greater proline level and in crops treated with proline under water deficit have been reported in…”
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Exogenous alpha lipoic acid can stimulate photosystem II activity and the gene expressions of carbon fixation and chlorophyll metabolism enzymes in maize seedlings under drought
Published in Journal of plant physiology (01-01-2019)“…Protective compounds such as non-enzymatic antioxidants, osmolytes and signal molecules have been applied to plants exposed to various environmental stresses…”
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SERPINB11 variant-related liver injury in STEC-HUS: case reports and literature review
Published in Pediatric nephrology (Berlin, West) (01-12-2022)“…Background Liver damage is uncommon in Shiga toxin-producing Escherichia coli– associated hemolytic uremic syndrome (STEC-HUS). Herein, we present two cases…”
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Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes
Published in Clinical neurology and neurosurgery (01-01-2024)Get full text
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A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy
Published in Clinical neurology and neurosurgery (01-06-2023)“…Mitochondrial neurogastrointestinal encephalopathy (MNGIE) is a well-known mitochondrial depletion syndrome. Since Van Goethem et al. described MNGIE syndrome…”
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Abscisic acid cross-talking with hydrogen peroxide and osmolyte compounds may regulate the leaf rolling mechanism under drought
Published in Acta physiologiae plantarum (01-08-2018)“…Leaf rolling observed in some crops such as maize, rice, wheat and sorghum is an indicator of decreased water status. Moderate leaf rolling not tightly or…”
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Prevalence of congenital sucrase-isomaltase deficiency in Turkey may be much higher than the estimates
Published in Journal of genetics (01-06-2023)“…Congenital sucrase–isomaltase deficiency (CSID) is a rare autosomal carbohydrate malabsorption disorder caused by mutations in the sucrase–isomaltase gene…”
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Diagnostic Workup and Micronutrient Deficiencies in Children With Failure to Thrive Without Underlying Diseases
Published in Nutrition in clinical practice (01-08-2019)“…Objectives and study Failure to thrive (FTT) is an interruption in the normal pattern of growth. We aimed to evaluate the clinical characteristics, underlying…”
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Assessment of cows milk‐related symptom scoring awareness tool in young Turkish children
Published in Journal of paediatrics and child health (01-11-2020)“…Background The diagnosis of cows milk protein allergy (CMPA) is not always easy. Cow's Milk‐related Symptom Score (CoMiSS) has been developed to raise the…”
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Very-early-onset Inflammatory Bowel Disease in an Infant with a Partial RIPK1 Deletion
Published in Journal of clinical immunology (01-06-2024)“…The monogenic causes of very-early-onset inflammatory bowel disease (VEO-IBD) have been defined by genetic studies, which were usually related to primary…”
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246 Allergy or Anaphylaxis?
Published in Archives of disease in childhood (11-10-2021)“…ObjectiveFood protein-induced enterocolitis syndrome (FPIES) is a non–IgE-mediated gastrointestinal food hypersensitivity manifesting as profuse repetitive…”
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Allogeneic hematopoietic stem cell and liver transplantation in a young girl with dedicator of cytokinesis 8 protein deficiency
Published in Pediatric transplantation (01-11-2019)“…DOCK8 deficiency is a rare inherited combined immunodeficiency, caused by mutations in the DOCK8 gene. We describe a case with DOCK8 deficiency associated with…”
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Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease: an open-label phase 2 and 3 study
Published in The Lancet (British edition) (17-02-2024)“…CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy (CHAPLE) is an ultra-rare genetic disorder…”
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Evaluation of malnutrition development risk in hospitalized children
Published in Nutrition (Burbank, Los Angeles County, Calif.) (01-04-2018)“…•Evaluation of the nutritional status of hospitalized children should be routinized.•Each hospitalized child should be evaluated by one of the scoring…”
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The frequency of Duchenne muscular dystrophy/Becker muscular dystrophy and Pompe disease in children with isolated transaminase elevation: results from the observational VICTORIA study
Published in Frontiers in pediatrics (25-09-2023)“…Introduction Elevated transaminases and/or creatine phosphokinase can indicate underlying muscle disease. Therefore, this study aims to determine the frequency…”
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Evaluation of children with chronic cough including obstructive sleep apnea: a single-center experience
Published in European journal of pediatrics (01-02-2019)“…Chronic cough in children may be due to a diverse range of etiologies. We aimed to evaluate children with chronic cough following a standardized cough…”
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