A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Medullary sponge kidney. NOTICE Undefined index: PDF (includes_ws_v2/controladores/[54]). HIPOKALIEMIA SINTOMÁTICA ASOCIADA A ENFERMEDAD DE CACCHI – RICCI. V. Esteve, N. Fontseré, A. Saurina, X. Cuevas. Read. Times was read.
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Specialised Social Services Eurordis directory. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Previous article Next article.
CiteScore measures average citations enfermedda per document published. The journal accepts submissions of articles in English and in Spanish languages. The journal accepts submissions of articles in English and in Spanish languages. Poster actions add bookmark contact presenter send a friend download pdf. Continuing navigation will be considered as acceptance of this use. Check this box if you wish to receive a copy of your facchi-ricci. The Journal publishes articles on basic or clinical research relating to nephrology, arterial hypertension, dialysis and kidney transplants.
Individuals with medullary sponge kidney are at increased risk for kidney stones and urinary tract infection uti. Also known as czcchi-ricci cacchiricci disease, medullary sponge kidney is a congenital developmental abnormality characterized by ectasia and cystic dilatation of the intrapyramidal or intrapapillary portions of the renal medullary collecting ducts.
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Medullary sponge kidney nord national organization for. Home Articles in press Enfermedaf. Pdf symptomatic hypokalemia associated with cacchiricci. Si continua navegando, consideramos que acepta su uso. Medullary sponge kidney also known as cacchiricci disease is a congenital disorder of the kidneys characterized by cystic dilatation of the collecting tubules in one or both kidneys. On the first click the button will be activated and you can then share the poster with a second click.
This item has received. It is governed by the peer review system and all original papers are subject to internal assessment and external reviews. In msk, tiny sacs called cysts form in the medulla the inner part of the kidney, creating a spongelike appearance. Medullary sponge kidney msk is a birth defect of the tubules tiny tubes inside the kidneys.
SRJ is a prestige metric based on the idea that not all citations are the same. Medullary sponge kidney is a benign congenital disorder characterized by dilatation of collecting tubules in 1 or more renal papillae, affecting 1 or both kidneys. National kidney foundation genetic and rare diseases. Summary and related texts. The documents contained in this web site are presented for information purposes only.
Ee ricci disease, precalyceal canalicular ectasia, cacchiricci syndrome, sponge kidney, cystic dilatation of renal collecting tubes megalocytic interstitial nephritis synonyms. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s enfermddad.
June Pages An Orphanet summary for this disease is currently under development. You can change the settings or obtain more information by clicking here. Si continua navegando, consideramos que acepta su uso.
HIPOKALIEMIA SINTOMÁTICA ASOCIADA A ENFERMEDAD DE CACCHI-RICCI | Nefrología (English Edition)
Other search option s Alphabetical list. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page. Home Articles in press Archive. This work is licensed under a Creative Commons Attribution 4. Are you a health professional able to prescribe or dispense drugs?
Medullary sponge kidney is usually a benign condition, and patients can remain asymptomatic. Subscribe to our Newsletter. It is governed by the peer review system and all original papers are subject to internal assessment and external reviews.
You can change the settings or obtain more information by clicking here. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. Medullary cystic kidney is a rare inherited kidney disease nephropathy characterized by excessive amounts of urea and other waste products in the urine uremia. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.
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Orphanet: Enfermedad de Cacchi Ricci
Interstitial megalocytic nephritis, transplant megalocytic interstitial nephritis type. Summary An Orphanet summary for this disease is currently under development. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. For all other comments, please send your remarks via contact us.