Results 281 to 290 of about 1,634,332 (380)

Use of Telenursing in the conservative treatment of patients with chronic renal insufficiency: scoping review. [PDF]

Rev Lat Am Enfermagem
Biancamano AO, Camacho ACLF, Cortez EA, Menezes HF, Almeida YS, Rocha CCDM.   +5 more
europepmc   +1 more source

Functional evaluation of penile hemodynamics [PDF]

, 1988
Bookstein, Brindley, Buvat, Ek, Jevtich, Juenemann, Jünemann, Karacan, Kockott, Lue, Lue, Newman, Porst, Sidi, Stief, van Arsdalen, Virag, Virag, Virag, Virag, Zorgniotti   +20 more
core   +1 more source

Efficacy of brivudine in the treatment of herpes zoster with diabetes and renal insufficiency following resection of left renal carcinoma: a case report

Yuren Zhang, Jie Li, Qing Ni
openalex   +1 more source

Relationship of estimated GFR and coronary artery calcification in the CRIC (Chronic Renal Insufficiency Cohort) Study.

American Journal of Kidney Diseases, 2011
M. Budoff, D. Rader, M. Reilly, E. Mohler, J. Lash, Wei Yang, L. Rosen, M. Glenn, V. Teal, H. Feldman   +9 more
semanticscholar   +1 more source

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

Analysis of efficacy factors in unilateral obstructive severe renal insufficiency: a single-centre retrospective study. [PDF]

BMC Nephrol
Li J, Pang H, Li W.
europepmc   +1 more source

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

Anticoagulant therapy in renal insufficiency theme: Anticoagulation in complex situations. [PDF]

Thromb Res
Parks AL, Stevens SM, Woller SC.
europepmc   +1 more source

P.021 RENAL INSUFFICIENCY IS ASSOCIATED WITH AUGMENTATION INDEX AND ENDOTHELIAL DYSFUNCTION

, 2007
J. Egresits, János Nemcsik, Taha El Hadj Othmane, Ervin Finta, Katalin Farkas, András Tislér, István Kiss   +6 more
openalex   +1 more source

Mechanisms of Mitochondrial Toxicity and Cytotoxicity Caused by Pseudomonas aeruginosa Pyocyanin in Human Nasal Epithelial Cells

International Forum of Allergy &Rhinology, EarlyView.
ABSTRACT Background Pseudomonas aeruginosa is an opportunistic pathogen in cystic fibrosis‐related chronic rhinosinusitis (CF‐CRS) that produces phenazine metabolites pyocyanin and 1‐hydroxyphenazine (1‐HP), which may have detrimental effects on mitochondria, reactive oxygen species (ROS), Ca2+ signaling, and apoptosis.
Joel C. Thompson, April Park, Yobouet Ines Kouakou, Zoey A. Miller, Nabil F. Darwich, Nithin D. Adappa, James N. Palmer, Ryan M. Carey, Robert J. Lee   +8 more
wiley   +1 more source