Results 231 to 240 of about 1,613,591 (292)

Residual Syntax score and percutaneous coronary intervention in diabetic patients with renal insufficiency. [PDF]

Am J Transl Res
Peng M, Ye T, Lan K, Xiong B, Xia L, Ding X, Wang C, Chen Y, Cai L.   +8 more
europepmc   +1 more source

Pharmacokinetics of polymyxin B in a patient with renal insufficiency: a case report.

Clinical Infectious Diseases, 2011
A. Kwa, Kamilia Abdelraouf, J. Low, V. Tam   +3 more
semanticscholar   +1 more source

A case of microscopic polyarteritis nodosa (microscopic PN) combined with severe pneumonorrhagia and subacute renal insufficiency.

, 1992
石田 和之, 古屋 徳郎, 筒井 秀人, 松田 治, 三宅 祥三, 戸村 成男   +5 more
openalex   +2 more sources

Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato, Naho Morisaki, Akinori Moriichi   +2 more
wiley   +1 more source

Population Pharmacokinetic/Pharmacodynamic Study of Linezolid in Hospital-Acquired Pneumonia Patients with Renal Insufficiency. [PDF]

Drug Des Devel Ther
Xu J, Chen X, Zhang Q, Zhuang Z, Yuan Y, Duan L, Shi L, Zhu C, Li J, Lu J, Yu Y, Tang L.   +11 more
europepmc   +1 more source

THE EFFECT OF HYDRATION AND PROSTAGLANDIN E1 FOR RENAL INSUFFICIENCY IN ARTERIOSCLEROSIS OBLITERANS

, 1991
Yoichi Tamura, Masato Furuyama, Sadanori Takeo   +2 more
openalex   +2 more sources

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Evaluation of anti-CD38 monoclonal antibody-based immunotherapy in multiple myeloma with renal insufficiency: a systematic review and meta-analysis. [PDF]

Ther Adv Hematol
Bai H, Zhang C, Zhao A, Tang W, Zhang L.
europepmc   +1 more source

Renal insufficiency : With aim of prevention and progress.1.Renal insufficiency.4.Renal function of old people and evaluation ( including obstructive renal disturbance ).

, 1993
成清 卓二
openalex   +2 more sources

Management of Cardiovascular Health Issues in Turner Syndrome: Expert Insights and Expanded Recommendations From the 2024 Guideline Development Team

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Turner syndrome (TS) is frequently complicated by congenital heart disease (CHD). While left‐sided lesions such as bicuspid aortic valve (BAV) and coarctation of the aorta are the most common structural heart lesions in TS, other anomalies, such as aortic arch malformations, hypoplastic left heart syndrome (HLHS), persistent left superior vena
Katya de Groote, Sheetal R. Patel, Kristian Havmand Mortensen, Isabel Witvrouwen, Anthonie Duijnhouwer, Nicole M. Brown, Jasmine Grewal, Kathryn C. Chatfield, Aaron T. Dorfman, Siddharth K. Prakash   +9 more
wiley   +1 more source