نتایج جستجو برای: nephrotic syn

تعداد نتایج: 13187  

Nephrotic syndrome is a rare manifestation of renal artery stenosis, presented mainly in adulthood. This is the report of a 4 months old boy admitted for hypertension and nephrotic syndrome. Left renal artery stenosis and renal hypoplasia were documented by laboratory and imaging studies. Proteinuria improved with medical treatment, with no need to surgical repair. Blood pressure remained norma...

2011
Nan Jiang Dayong Xue Hongxiang Han

The genus Biston Leach, 1815 is reviewed for China. Seventeen species are recognized, of which Biston mediolatasp. n. is described. Biston pustulata (Warren, 1896) and Biston panterinariaexanthemata (Moore, 1888) are newly recorded for China. The following new synonyms are established: Biston suppressaria suppressaria (Guenée, 1858) (= Biston suppressaria benescripta (Prout, 1915), syn. n. = Bi...

2018
Seiji Kaji Takakuni Maki Hisanori Kinoshita Norihito Uemura Takashi Ayaki Yasuhiro Kawamoto Takahiro Furuta Makoto Urushitani Masato Hasegawa Yusuke Kinoshita Yuichi Ono Xiaobo Mao Tran H. Quach Kazuhiro Iwai Valina L. Dawson Ted M. Dawson Ryosuke Takahashi

Glial cytoplasmic inclusions (GCIs), commonly observed as α-synuclein (α-syn)-positive aggregates within oligodendrocytes, are the pathological hallmark of multiple system atrophy. The origin of α-syn in GCIs is uncertain; there is little evidence of endogenous α-syn expression in oligodendrocyte lineage cells, oligodendrocyte precursor cells (OPCs), and mature oligodendrocytes (OLGs). Here, ba...

2011
Eliezer Masliah Edward Rockenstein Michael Mante Leslie Crews Brian Spencer Anthony Adame Christina Patrick Margarita Trejo Kiren Ubhi Troy T. Rohn Sarah Mueller-Steiner Peter Seubert Robin Barbour Lisa McConlogue Manuel Buttini Dora Games Dale Schenk

Dementia with Lewy bodies (DLB) and Parkinson's Disease (PD) are common causes of motor and cognitive deficits and are associated with the abnormal accumulation of alpha-synuclein (α-syn). This study investigated whether passive immunization with a novel monoclonal α-syn antibody (9E4) against the C-terminus (CT) of α-syn was able to cross into the CNS and ameliorate the deficits associated wit...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Youngshin Lim Victoria M Kehm Edward B Lee James H Soper Chi Li John Q Trojanowski Virginia M-Y Lee

Abnormally accumulated α-synuclein (α-syn) is a pathological hallmark of Lewy body-related disorders such as Parkinson's disease (PD) and dementia with Lewy body disease (DLB). However, it is not well understood whether and how abnormal accumulation of α-syn leads to cognitive impairment or dementia in PD and DLB. Furthermore, it is not known whether targeted removal of α-syn pathology can reve...

Journal: :Cureus 2023

Nephrotic syndrome in pregnancy is associated with challenges for both patients and physicians. Early recognition crucial, when appropriate, renal biopsy should be considered to differentiate preeclampsia from other causes of glomerulopathies. Pregnancy a woman nephrotic high risk, more data are needed highlight outcomes.

2015
Mathieu Bourdenx Sandra Dovero Michel Engeln Simone Bido Matthieu F. Bastide Nathalie Dutheil Isabel Vollenweider Laetitia Baud Camille Piron Virginie Grouthier Thomas Boraud Grégory Porras Qin Li Veerle Baekelandt Dieter Scheller Anne Michel Pierre-Olivier Fernagut François Georges Grégoire Courtine Erwan Bezard Benjamin Dehay

INTRODUCTION Parkinson's disease (PD) is a progressive neurodegenerative disorder characterized by the loss of dopaminergic neurons as well as the presence of proteinaceous inclusions named Lewy bodies. α-synuclein (α-syn) is a major constituent of Lewy bodies, and the first disease-causing protein characterized in PD. Several α-syn-based animal models of PD have been developed to investigate t...

Journal: :Biomedicines 2023

Proteinuria is known to be associated with all-cause and cardiovascular mortality, nephrotic syndrome defined by the level of proteinuria hypoalbuminemia. With advances in medicine, new causative genes for genetic kidney diseases are being discovered increasingly frequently. We reviewed articles on proteinuria/nephrotic syndrome, focal segmental glomerulosclerosis, membranous nephropathy, diabe...

Journal: :Journal of the American Society of Nephrology : JASN 2005
Steven W Kraft Melvin M Schwartz Stephen M Korbet Edmund J Lewis

A series of patients with systemic lupus erythematosus (SLE) and proteinuria were studied to determine whether nephrotic-range proteinuria was associated with diffuse epithelial cell foot process effacement in the absence of peripheral glomerular immune aggregate deposition. Biopsies from patients with known or suspected SLE and a histologic diagnosis of (1) normal by light microscopy, (2) mesa...

Journal: :Lancet 2003
Allison A Eddy Jordan M Symons

Childhood nephrotic syndromes are most commonly caused by one of two idiopathic diseases: minimal-change nephrotic syndrome (MCNS) and focal segmental glomerulosclerosis (FSGS). A third distinct type, membranous nephropathy, is rare in children. Other causes of isolated nephrotic syndrome can be subdivided into two major categories: rare genetic disorders, and secondary diseases associated with...

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