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14 resultados encontrados.

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Hereditary Renal Cystic Diseases
Artículo
Acceso abierto Artículo DOAJ
Alper UZAK et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Polycystic kidney disease is one of the most common reasons of end stage renal failure. Polycystic kidney disease may result from many etiological factors, but frequently arises hereditarily. Autosomal dominant polycysti...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
Coronary Artery Disease Risk Factors in Patients on Continuous Ambulatory Peritoneal Dialysis
Artículo
Material complementario disponible Artículo DOAJ
Bekir POÇAN et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
AIM: We aimed to investigate especially early stage non traditional cardiovascular risk factors in end stage renal failure patients who were in Continued Ambulatory Peritoneal Dialysis (CAPD) programme in our center. M...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Material complementario disponibleEl enlace apunta a material asociado, anexos, tablas, datos o página complementaria. No se marca como libro/texto completo.
Material complementario
Demographic and Clinical Characteristics of Patients with Autosomal Dominant Polycystic Kidney Disease: A Single Center Experience
Artículo
Material complementario disponible Artículo DOAJ
Abdülmecit YILDIZ et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
OBJECTIVE: Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common hereditary kidney disease. We presented the ADPKD patients who were not undergoing replacement therapy. MATERIAL and METHODS: Accordin...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Material complementario disponibleEl enlace apunta a material asociado, anexos, tablas, datos o página complementaria. No se marca como libro/texto completo.
Material complementario
Inherited Podocyte Diseases
Artículo
Acceso abierto Artículo DOAJ2 fuentes relacionadas
Zeynep BİRSİN ÖZÇAKAR et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Podocytes are present in the glomerular capillary wall and they are the target cells injured in many diseases. In the past few years genetic studies performed especially in the familial nephrotic syndrome cases have shed...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
Urinary Findings and Biomarkers in Autosomal Dominant Polycystic Kidney Disease
Artículo
Acceso abierto Artículo DOAJ
İsmail Koçyiğit et al · Turkish Society of Nephrology · 2020 · ISSN 2667-4440
Autosomal dominant polycystic kidney disease (ADPKD), characterized by the development of multiple cysts in the kidneys and other organs, is the most common hereditary renal disorder and the fourth leading cause of end-s...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
Cystic Renal Disease in Children: A Broad Spectrum from Simple Cyst to End Stage Renal Failure
Artículo
Material complementario disponible Artículo DOAJ
Neslihan Çiçek et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Objective: Renal cystic diseases consist of a broad spectrum of hereditary or acquired conditions that may lead to end stage renal disease. We aimed to evaluate our patients diagnosed as renal cystic disease in terms of ...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Material complementario disponibleEl enlace apunta a material asociado, anexos, tablas, datos o página complementaria. No se marca como libro/texto completo.
Material complementario
Alport’s Syndrome
Artículo
Acceso abierto Artículo DOAJ
Tayfun AKALIN et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Alport’s syndrome is a hereditary kidney disease, frequently associated with hearing loss and ocular abnormalities. Type IV collagen is the main constituent of the basement membranes. Mutations in the COL4A3, COL4A4 an...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
CHRONIC RENAL FAILURE DUE TO FAMILIAL HYPOMAGNESEMIC HYPERCALCIURIA (A CASE REPORT)
Artículo
Acceso abierto Artículo DOAJ
Ali Rıza ODABAŞ et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Familial Hypomagnesemia- hypercalciuria is a hereditary disease of unknown etiology characterized by persistant Hypomagnesemia, incomplete distal tubuler acidosis, hypercalciuria and nephrocalcinosis. We have reported an...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
Colchicine-and Clarithromycin-Induced Rhabdomyolysis in a Hemodialysis Patient with Familial Mediterranean Fever
Artículo
Acceso abierto Artículo DOAJ
Amir Hossein ABEDİ et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Familial Mediterranean fever (FMF) is an autosomal recessive hereditary disease characterized by recurrent attacks of fever, usually accompanied by sterile polyserositis. Although colchicine is the main medical treatment...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
Evaluation of Genotypic and Phenotypic Characteristics of Children with Familial Mediterranean Fever in Eastern Turkey
Artículo
Acceso abierto Artículo DOAJ
Hülya KALEM et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Objective: Familial Mediterranean fever (FMF) is a hereditary disease. It usually affects countries in the Mediterranean region and is common in Turks. This retrospective study was conducted to evaluate phenotype-genotyp...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
FAMILIAL MEDITERRANEAN FEVER AND AMILOIDOSIS IN TURKISH MEDICINE
Artículo
Acceso abierto Artículo DOAJ
Emel ÖRÜN et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
In this report, by the guidance of Turkish and international literature, the features of FMF disease in Turkish patients and the advances in related with thi disease Turkish Medicine were presented. FMF is an autosomal r...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
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Open Access
Membranoproliferative Glomerulonephritis: The Most Common Pediatric Renal Pathology at a Tertiary Center in Turkey
Artículo
Acceso abierto Artículo DOAJ
Serra Sürmeli Döven et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Objective: This study aimed to assess the histopathological diagnosis of pediatric renal biopsies performed at the tertiary referral center in the city and to compare the ultrasound (USG) -guided biopsy and percutaneous ...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
Recurrent Hypokalemia, Hypomagnesemia and Metabolic Alkalosis Following Preemptive Renal Transplantation: Bartter Syndrome
Artículo
Acceso abierto Artículo DOAJ
Simge BARDAK et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
Native kidney function can still contribute to the total renal function after preemptive renal transplantation, and the primary problems of native kidneys such as tubular disorders may persist or reappear in the post-tra...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access
THE ETIOLOGIC EVALUATION IN PATIENTS WITH CHRONIC RENAL FAILURE
Artículo
Acceso abierto Artículo DOAJ
Harika ALPAY et al · Turkish Society of Nephrology · 2019 · ISSN 2667-4440
A retrospective analysis of pediatric cases of chronic renal failure (CRF) was performed at our hospital over 2 years period. The diagnosis of CRF was based on gomerular filtration rate less than 50 ml/min per 1.73 m2 bo...
LCC LCC:Internal medicine; TENDOlBlZGlhdHJpY3M~Idioma eng
Acceso abiertoRuta libre sin proxy. Acceso recomendado cuando no hay suscripción activa.
Open Access