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1. 成人における尿蛋白排泄量の評価および非ネフローゼ域蛋白尿のみの評価 assessment of urinary protein excretion and evaluation of isolated non nephrotic proteinuria in adults
2. 小児における蛋白尿の評価 evaluation of proteinuria in children
3. 重症蛋白尿およびネフローゼ症候群の概要 overview of heavy proteinuria and the nephrotic syndrome
4. 起立性（体位性）蛋白尿症 orthostatic postural proteinuria
5. 妊娠中の蛋白尿：評価およびマネージメント proteinuria in pregnancy evaluation and management

Vascular and parenchymal lesions along with enhanced neurogenesis characterize the brain of asymptomatic stroke-prone spontaneous hypertensive rats.

Cova L, Gelosa P, Mura E, Mauro A, Stramba-Badiale M, Michailidis G, Colonna A, El Assawy N, Pignieri A, Busca G, Tremoli E, Silani V, Sironi L, Zanchetti A.SourceaDepartment of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano bDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milan cLaboratory of Neurobiology, Istituto Auxologico Italiano, S. Giuseppe Hospital, Piancavallo di Oggebbio (VB) dDepartment of Neuroscience, University of Turin, Turin eDepartment of Geriatrics and Cardiovascular Medicine, IRCCS Istituto Auxologico Italiano fDepartment of Clinical Sciences and Community Health, University of Milan, Cardiovascular Medicine, Fondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico gIRCCS Centro Cardiologico Monzino hDepartment of Pathophysiology and Transplantation, 'Dino Ferrari' Centre, University of Milan iIRCCS Istituto Auxologico Italiano and University of Milan, Milan, Italy *Lidia Cova, Paolo Gelosa, Elena Mura, and Luigi Sironi contributed equally to the study reported in this article.
Journal of hypertension.J Hypertens.2013 Aug;31(8):1618-1628.
BACKGROUND AND OBJECTIVES:: Spontaneously hypertensive stroke-prone rats (SHRSPs) develop hypertension, cerebrovascular abnormalities and a stroke phenotype in association with higher levels of proteinuria. Here, we focus on cerebral abnormalities preceding lesions detectable by MRI.METHODS:: Longit
PMID 23666422

A Rare Case of Type I RenalTubular Acidosis with Membranous Nephropathy Presenting as Hypokalemic Paralysis.

Sunder S, Sathi S, Venkataramanan K, Verma H, Bhardwaj M, Rajesh J, Mahapatra H.SourceDepartment of Nephrology, PGIMER, Dr. R.M.L. Hospital, New Delhi, India.
Case reports in nephrology and urology.Case Rep Nephrol Urol.2013 Jul 1;3(2):91-8. doi: 10.1159/000353768. Print 2013 Jun.
Type 1 renal tubular acidosis (RTA), or distal RTA (dRTA), is a disorder of renal tubular acidification, which is generally asymptomatic but may rarely present as hypokalemic paralysis. Here, we report the case of a young male who presented with sudden onset weakness of all 4 limbs and a 2-month his
PMID 23898345

Ponticelli C, Glassock RJ.SourceDivision of Nephrology, IRCCS Humanitas Hospital, Rozzano, Milan, Italy, †David Geffen School of Medicine, University of California, Los Angeles, California.
Clinical journal of the American Society of Nephrology : CJASN.Clin J Am Soc Nephrol.2013 Jun 27. [Epub ahead of print]
Membranous nephropathy (MN) is an autoimmune disease usually associated with a nephrotic syndrome and it may progress to ESRD in the long term. Its etiology is often unknown (idiopathic MN), whereas other cases have a recognizable etiology (secondary MN). In idiopathic MN, the glomerular lesions are
PMID 23813556

Association of Kidney Dysfunction With Asymptomatic Cerebrovascular Abnormalities in a Japanese Population With Health Checkups

Circulation journal : official journal of the Japanese Circulation Society 81(8), 1191-1197, 2017-08
NAID 40021261525

Association of Kidney Dysfunction With Asymptomatic Cerebrovascular Abnormalities in a Japanese Population With Health Checkups

Second-trimester urine nephrin:creatinine ratio versus soluble fms-like tyrosine kinase-1:placental growth factor ratio for prediction of preeclampsia among asymptomatic women