000 03660cam a2200217 4500
001 9780323462488
008 220107t2016 xxu||||| |||| 00| 0 eng d
020 _a9780323462488
020 _a9780323390538
041 _aeng
100 _aKashgarian, Michael.
245 0 _aDiagnostic Atlas of Renal Pathology.
250 _a3rd ed.
260 _aPhiladelphia :
_bElsevier Health Sciences,
_c2016
300 _a1 online resource (565 pages)
505 _aFront Cover; IFC; DIAGNOSTIC ATLAS OF RENAL PATHOLOGY; DIAGNOSTIC ATLAS OF RENAL PATHOLOGY; Copyright; Preface; Acknowledgments; Contents; DIAGNOSTIC ATLAS OF RENAL PATHOLOGY; 1 -- Approach to Diagnosis of the Kidney Biopsy; 2 -- Normal Growth and Maturation; 3 -- Glomerular Diseases; Glomerular Diseases That Cause Nephrotic Syndrome: Non-Immune Complex; MINIMAL CHANGE DISEASE AND FOCAL SEGMENTAL GLOMERULOSCLEROSIS: INTRODUCTION; MINIMAL CHANGE DISEASE; Etiology/Pathogenesis; FOCAL SEGMENTAL GLOMERULOSCLEROSIS; Diagnosis of Recurrence of FSGS in the Transplant; Etiology/Pathogenesis.;Collapsing GlomerulopathyEtiology/Pathogenesis; Tip Lesion Variant of FSGS; Etiology/Pathogenesis; Cellular Variant of FSGS; Etiology/Pathogenesis; Perihilar Variant of FSGS; Etiology/Pathogenesis-Secondary Forms of FSGS; CONGENITAL NEPHROTIC SYNDROME OF FINNISH TYPE; Etiology/Pathogenesis; DIFFUSE MESANGIAL SCLEROSIS; Frasier Syndrome; Etiology/Pathogenesis; Glomerular Diseases That Cause Nephrotic/Nephritic Syndrome: Complement Related; C1Q NEPHROPATHY; Etiology/Pathogenesis; C3 GLOMERULOPATHIES; Dense Deposit Disease; Etiology/Pathogenesis; C3 Glomerulonephritis; Etiology/Pathogenesis.;Glomerular Diseases That Cause Nephrotic Syndrome: Immune ComplexMEMBRANOUS NEPHROPATHY; Etiology/Pathogenesis; MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS; Etiology/Pathogenesis; FIBRILLARY GLOMERULONEPHRITIS; Etiology/Pathogenesis; IMMUNOTACTOID GLOMERULOPATHY; Etiology/Pathogenesis; Glomerular Diseases That Cause Hematuria or Nephritic Syndrome: Immune Complex; ACUTE POSTINFECTIOUS GLOMERULONEPHRITIS; Etiology/Pathogenesis; IGA NEPHROPATHY; Etiology/Pathogenesis; Secondary Glomerular Diseases; Diseases Associated With Nephrotic Syndrome; MONOCLONAL IMMUNOGLOBULIN DEPOSITION DISEASE.;Light Chain Deposition DiseaseLight and Heavy Chain Deposition Disease and Heavy Chain Deposition Disease; Etiology/Pathogenesis of MIDD; AMYLOIDOSIS; Etiology/Pathogenesis; PROLIFERATIVE GLOMERULONEPHRITIS WITH MONOCLONAL DEPOSITS; Etiology/Pathogenesis; HIV-ASSOCIATED NEPHROPATHY; Etiology/Pathogenesis; SICKLE CELL NEPHROPATHY; Etiology/Pathogenesis; FABRY DISEASE; Etiology/Pathogenesis; LIPOPROTEIN GLOMERULOPATHY; LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) DEFICIENCY; Etiology/Pathogenesis; HEREDITARY FOCAL SEGMENTAL GLOMERULOSCLEROSIS.;Diseases Associated With Nephritic Syndrome or Rapidly Progressive Glomerulonephritis (RPGN): Immune MediatedLUPUS NEPHRITIS; Histopathology; Class I Minimal Mesangial Lupus Nephritis; Class II Mesangial Proliferative Lupus Nephritis; Class III Focal Lupus Nephritis; Class IV Diffuse Lupus Nephritis; Class V Membranous Lupus Nephritis; Class VI Advanced Sclerosing Lupus Nephritis; ATYPICAL PRESENTATIONS OF RENAL INVOLVEMENT IN SLE; Lupus Podocytopathy/Minimal Change Disease; ANCA-Associated Nephritis; Mixed Patterns and Transformation; Immunofluorescence Microscopic Features.
520 _aPractical, highly visual guidance for efficient, accurate diagnosis of renal disease.
690 _aRenal pharmacology.
856 _uhttps://go.openathens.net/redirector/nhs?url=https://www.clinicalkey.com/dura/browse/bookChapter/3-s2.0-C20140032650
999 _c58589
_d58589