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[Thrombotic microangiopathy/haemolytic uraemic syndrome. Histopathology update].

Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia

Vazquez Martul E.
PMID: 30012310
Rev Esp Patol. 2018 Jul - Sep;51(3):170-177. doi: 10.1016/j.patol.2017.10.007. Epub 2017 Dec 16.

Thrombotic microangiopathy (TMA) encompasses different entities known as haemolytic uraemic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP). The histopathological characteristics have remained constant since the initial description and consist in glomerular-type affectation with the presence of double contours, mesangiolysis...

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Vazquez Martul E. Microangiopatía trombótica/síndrome hemolítico urémico. Actualización de sus características histopatológicas. [Thrombotic microangiopathy/haemolytic uraemic syndrome. Histopathology update]. Rev Esp Patol. 2017;51(3):170-177doi: 10.1016/j.patol.2017.10.007.
Vazquez Martul, E. (2018). Microangiopatía trombótica/síndrome hemolítico urémico. Actualización de sus características histopatológicas. [Thrombotic microangiopathy/haemolytic uraemic syndrome. Histopathology update]. Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia, 51(3), 170-177. https://doi.org/10.1016/j.patol.2017.10.007
Vazquez Martul, Eduardo. "Microangiopatía trombótica/síndrome hemolítico urémico. Actualización de sus características histopatológicas." [Thrombotic microangiopathy/haemolytic uraemic syndrome. Histopathology update]. Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia vol. 51,3 (2018): 170-177. doi: https://doi.org/10.1016/j.patol.2017.10.007
Vazquez Martul E. Microangiopatía trombótica/síndrome hemolítico urémico. Actualización de sus características histopatológicas. [Thrombotic microangiopathy/haemolytic uraemic syndrome. Histopathology update]. Rev Esp Patol. 2018 Jul - Sep;51(3):170-177. doi: 10.1016/j.patol.2017.10.007. Epub 2017 Dec 16. Spanish. PMID: 30012310.
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Atypical haemolytic uremic syndrome: when multiple etiologies meet.

International urology and nephrology

Barbieri D, García-Prieto A, Verde E, Goicoechea M, Luño J.
PMID: 30251008
Int Urol Nephrol. 2018 Nov;50(11):2109-2110. doi: 10.1007/s11255-018-1980-0. Epub 2018 Sep 24.

No abstract available.

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Barbieri D, García-Prieto A, Verde E, et al. Atypical haemolytic uremic syndrome: when multiple etiologies meet. Int Urol Nephrol. 2018;50(11):2109-2110doi: 10.1007/s11255-018-1980-0.
Barbieri, D., García-Prieto, A., Verde, E., Goicoechea, M., & Luño, J. (2018). Atypical haemolytic uremic syndrome: when multiple etiologies meet. International urology and nephrology, 50(11), 2109-2110. https://doi.org/10.1007/s11255-018-1980-0
Barbieri, D, et al. "Atypical haemolytic uremic syndrome: when multiple etiologies meet." International urology and nephrology vol. 50,11 (2018): 2109-2110. doi: https://doi.org/10.1007/s11255-018-1980-0
Barbieri D, García-Prieto A, Verde E, Goicoechea M, Luño J. Atypical haemolytic uremic syndrome: when multiple etiologies meet. Int Urol Nephrol. 2018 Nov;50(11):2109-2110. doi: 10.1007/s11255-018-1980-0. Epub 2018 Sep 24. PMID: 30251008.
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Severe hypertension with renal thrombotic microangiopathy: what happened to the usual suspect?.

Kidney international

Van Laecke S, Van Biesen W.
PMID: 28501299
Kidney Int. 2017 Jun;91(6):1271-1274. doi: 10.1016/j.kint.2017.02.025.

Patients with atypical hemolytic uremic syndrome (aHUS) and malignant hypertension can both present with concomitant hypertension and thrombotic microangiopathy (TMA), rendering policy decisions complex. Timmermans et al. report that patients with severe hypertension and renal TMA might have unrecognized...

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Van Laecke S, Van Biesen W. Severe hypertension with renal thrombotic microangiopathy: what happened to the usual suspect?. Kidney Int. 2017;91(6):1271-1274doi: 10.1016/j.kint.2017.02.025.
Van Laecke, S., & Van Biesen, W. (2017). Severe hypertension with renal thrombotic microangiopathy: what happened to the usual suspect?. Kidney international, 91(6), 1271-1274. https://doi.org/10.1016/j.kint.2017.02.025
Van Laecke, Steven, and Van Biesen, Wim. "Severe hypertension with renal thrombotic microangiopathy: what happened to the usual suspect?." Kidney international vol. 91,6 (2017): 1271-1274. doi: https://doi.org/10.1016/j.kint.2017.02.025
Van Laecke S, Van Biesen W. Severe hypertension with renal thrombotic microangiopathy: what happened to the usual suspect?. Kidney Int. 2017 Jun;91(6):1271-1274. doi: 10.1016/j.kint.2017.02.025. PMID: 28501299.
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Atypical hemolytic uremic syndrome: from diagnosis to treatment.

Clinical chemistry and laboratory medicine

Franchini M.
PMID: 25803082
Clin Chem Lab Med. 2015 Oct;53(11):1679-88. doi: 10.1515/cclm-2015-0024.

Thrombotic microangiopathy (TMA) is a relatively rare condition but a medical urgency requiring immediate intervention to avoid irreversible organ damage or death. Symptoms on presentation include microangiopathic haemolytic anaemia, thrombocytopenia and organ damage. The most frequent direct causes of...

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Franchini M. Atypical hemolytic uremic syndrome: from diagnosis to treatment. Clin Chem Lab Med. 2015;53(11):1679-88doi: 10.1515/cclm-2015-0024.
Franchini, M. (2015). Atypical hemolytic uremic syndrome: from diagnosis to treatment. Clinical chemistry and laboratory medicine, 53(11), 1679-88. https://doi.org/10.1515/cclm-2015-0024
Franchini, Massimo. "Atypical hemolytic uremic syndrome: from diagnosis to treatment." Clinical chemistry and laboratory medicine vol. 53,11 (2015): 1679-88. doi: https://doi.org/10.1515/cclm-2015-0024
Franchini M. Atypical hemolytic uremic syndrome: from diagnosis to treatment. Clin Chem Lab Med. 2015 Oct;53(11):1679-88. doi: 10.1515/cclm-2015-0024. PMID: 25803082.
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Rare and Complex: lessons from a cohort of patients with Atypical Hemolytic Uremic Syndrome.

Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia

Palma LMP.
PMID: 34057986
J Bras Nefrol. 2021 Jul-Sep;43(3):295-296. doi: 10.1590/2175-8239-JBN-2021-0066.

No abstract available.

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Palma LMP. Rare and Complex: lessons from a cohort of patients with Atypical Hemolytic Uremic Syndrome. J Bras Nefrol. 2021;43(3):295-296doi: 10.1590/2175-8239-JBN-2021-0066.
Palma, L. M. P. (2021). Rare and Complex: lessons from a cohort of patients with Atypical Hemolytic Uremic Syndrome. Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia, 43(3), 295-296. https://doi.org/10.1590/2175-8239-JBN-2021-0066
Palma, Lilian Monteiro Pereira. "Rare and Complex: lessons from a cohort of patients with Atypical Hemolytic Uremic Syndrome." Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia vol. 43,3 (2021): 295-296. doi: https://doi.org/10.1590/2175-8239-JBN-2021-0066
Palma LMP. Rare and Complex: lessons from a cohort of patients with Atypical Hemolytic Uremic Syndrome. J Bras Nefrol. 2021 Jul-Sep;43(3):295-296. doi: 10.1590/2175-8239-JBN-2021-0066. Portuguese. PMID: 34057986; PMCID: PMC8428645.
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Clinical guides for atypical hemolytic uremic syndrome in Japan.

Pediatrics international : official journal of the Japan Pediatric Society

Kato H, Nangaku M, Hataya H, Sawai T, Ashida A, Fujimaru R, Hidaka Y, Kaname S, Maruyama S, Yasuda T, Yoshida Y, Ito S, Hattori M, Miyakawa Y, Fujimura Y, Okada H, Kagami S.
PMID: 27460397
Pediatr Int. 2016 Jul;58(7):549-55. doi: 10.1111/ped.13044.

Atypical hemolytic uremic syndrome (aHUS) is a rare disease characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. In 2013, we developed diagnostic criteria to enable early diagnosis and timely initiation of appropriate treatment for...

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Kato H, Nangaku M, Hataya H, et al. Clinical guides for atypical hemolytic uremic syndrome in Japan. Pediatr Int. 2016;58(7):549-55doi: 10.1111/ped.13044.
Kato, H., Nangaku, M., Hataya, H., Sawai, T., Ashida, A., Fujimaru, R., Hidaka, Y., Kaname, S., Maruyama, S., Yasuda, T., Yoshida, Y., Ito, S., Hattori, M., Miyakawa, Y., Fujimura, Y., Okada, H., Kagami, S. (2016). Clinical guides for atypical hemolytic uremic syndrome in Japan. Pediatrics international : official journal of the Japan Pediatric Society, 58(7), 549-55. https://doi.org/10.1111/ped.13044
Kato, Hideki, et al. "Clinical guides for atypical hemolytic uremic syndrome in Japan." Pediatrics international : official journal of the Japan Pediatric Society vol. 58,7 (2016): 549-55. doi: https://doi.org/10.1111/ped.13044
Kato H, Nangaku M, Hataya H, Sawai T, Ashida A, Fujimaru R, Hidaka Y, Kaname S, Maruyama S, Yasuda T, Yoshida Y, Ito S, Hattori M, Miyakawa Y, Fujimura Y, Okada H, Kagami S. Clinical guides for atypical hemolytic uremic syndrome in Japan. Pediatr Int. 2016 Jul;58(7):549-55. doi: 10.1111/ped.13044. PMID: 27460397.
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A new therapeutic strategy for atypical HUS.

Blood

Moake JL.
PMID: 28729338
Blood. 2017 Jul 20;130(3):243-244. doi: 10.1182/blood-2017-06-783704.

No abstract available.

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Moake JL. A new therapeutic strategy for atypical HUS. Blood. 2017;130(3):243-244doi: 10.1182/blood-2017-06-783704.
Moake, J. L. (2017). A new therapeutic strategy for atypical HUS. Blood, 130(3), 243-244. https://doi.org/10.1182/blood-2017-06-783704
Moake, Joel L. "A new therapeutic strategy for atypical HUS." Blood vol. 130,3 (2017): 243-244. doi: https://doi.org/10.1182/blood-2017-06-783704
Moake JL. A new therapeutic strategy for atypical HUS. Blood. 2017 Jul 20;130(3):243-244. doi: 10.1182/blood-2017-06-783704. PMID: 28729338.
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Showing 1 to 7 of 7 entries