Mayo Clinic
Pathology
Dr. Samih H. Nasr, MD
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Samih Nasr practices Pathology. Samih Nasr is also a published doctor. He has 100 publication published. The most recent publication is: The clinicopathologic characteristics and outcome of atypical anti-glomerular basement membrane nephritis. Doctor Samih H. Nasr, MD is registered with Medicare and accepts Medicare payments.
Publications
- The clinicopathologic characteristics and outcome of atypical anti-glomerular basement membrane nephritis.
- A Patient with Abnormal Kidney Function and a Monoclonal Light Chain in the Urine.
- Rapidly progressive glomerulonephritis due to coexistent anti-glomerular basement membrane disease and fibrillary glomerulonephritis.
- Leukocyte chemotactic factor 2 amyloidosis (ALECT2) is a common form of renal amyloidosis among Egyptians.
- Leukocyte Cell-Derived Chemotaxin 2-Associated Amyloidosis: A Recently Recognized Disease with Distinct Clinicopathologic Characteristics.
- Disappearance of immunoglobulins from persistent renal amyloid deposits following stem cell transplantation for heavy-and light-chain amyloidosis.
- Update on endocarditis-associated glomerulonephritis.
- Diagnosis of monoclonal gammopathy of renal significance.
- Focal and segmental glomerulosclerosis: clinical and kidney biopsy correlations.
- Crystalglobulin-Induced Nephropathy.
- Clinical characteristics, causes and outcomes of acute interstitial nephritis in the elderly.
- Membranoproliferative glomerulonephritis associated with autoimmune diseases.
- Characterization and outcomes of renal leukocyte chemotactic factor 2-associated amyloidosis.
- Utility of Urine Eosinophils in the Diagnosis of Acute Interstitial Nephritis.
- Disseminated microsporidiosis in a renal transplant recipient: case report and review of the literature.
- Renal Amyloidosis: Origin and Clinicopathologic Correlations of 474 Recent Cases.
- Membranous glomerulonephritis is a manifestation of IgG4-related disease.
- Laser Microdissection and Proteomic Analysis of Amyloidosis, Cryoglobulinemic GN, Fibrillary GN, and Immunotactoid Glomerulopathy.
- The diagnosis and characteristics of renal heavy-chain and heavy/light-chain amyloidosis and their comparison with renal light-chain amyloidosis.
- Low- and high-molecular-weight urinary proteins as predictors of response to rituximab in patients with membranous nephropathy: a prospective study.
- Bacterial infection-related glomerulonephritis in adults.
- Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.
- Urinary Albumin Excretion Patterns of Patients with Cast Nephropathy and Other Monoclonal Gammopathy-Related Kidney Diseases.
- C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up.
- Clinicopathologic correlations in multiple myeloma: a case series of 190 patients with kidney biopsies.
- Laser microdissection and mass spectrometry-based proteomics aids the diagnosis and typing of renal amyloidosis.
- Myoglobin-Associated Acute Kidney Injury in the Setting of Ciprofloxacin Administration.
- Renal Monoclonal Immunoglobulin Deposition Disease: A Report of 64 Patients from a Single Institution.
- Clinical features of patients with immunoglobulin light chain amyloidosis (AL) with vascular-limited deposition in the kidney.
- COMPARISON of Human Papillomavirus Testing and Cytology for Cervical Cancer Screening in a Primary Health Care Setting in the Democratic Republic of Congo.
- Renal crescentic alpha heavy chain deposition disease: a report of 3 cases and review of the literature.
- Acquired glomerular lesions in patients with Down syndrome.
- Diagnosis of IgG4-Related Tubulointerstitial Nephritis.
- IgA-Dominant Postinfectious Glomerulonephritis: A New Twist on an Old Disease.
- Myeloproliferative neoplasms cause glomerulopathy.
- Proliferative glomerulonephritis secondary to dysfunction of the alternative pathway of complement.
- Fibrillary glomerulonephritis: a report of 66 cases from a single institution.
- A Novel Mutation of LAMB2 in a Multigenerational Mennonite Family Reveals a New Phenotypic Variant of Pierson Syndrome.
- Postinfectious glomerulonephritis in the elderly.
- Proliferative glomerulonephritis with monoclonal IgG deposits recurs in the allograft.
- Mass spectrometry-based proteomic diagnosis of renal immunoglobulin heavy chain amyloidosis.
- Prkdc participates in mitochondrial genome maintenance and prevents Adriamycin-induced nephropathy in mice.
- A molecular profile of focal segmental glomerulosclerosis from formalin-fixed, paraffin-embedded tissue.
- C1q deposition in the renal allograft: a report of 24 cases.
- Incompletely penetrant PKD1 alleles mimic the renal manifestations of ARPKD.
- Treatment with IFN-{alpha}, -{beta}, or -{gamma} is associated with collapsing focal segmental glomerulosclerosis.
- Proliferative glomerulonephritis with monoclonal IgG deposits.
- Membranous glomerulonephritis with ANCA-associated necrotizing and crescentic glomerulonephritis.
- Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients.
- Oxalate nephropathy complicating Roux-en-Y Gastric Bypass: an underrecognized cause of irreversible renal failure.
- Pauci-immune crescentic glomerulonephritis superimposed on diabetic glomerulosclerosis.
- Necrotizing and crescentic lupus nephritis with antineutrophil cytoplasmic antibody seropositivity.
- Acute postinfectious glomerulonephritis in the modern era: experience with 86 adults and review of the literature.
- Nodular glomerulosclerosis in the nondiabetic smoker.
- Upregulation of EphA2 during in vivo and in vitro renal ischemia-reperfusion injury: role of Src kinases.
- Immunization with an apoptotic cell-binding protein recapitulates the nephritis and sequential autoantibody emergence of systemic lupus erythematosus.
- Visual inspection as a cervical cancer screening method in a primary health care setting in Africa.
- Hereditary nephritis mimicking immune complex-mediated glomerulonephritis.
- Differential protective effects of volatile anesthetics against renal ischemia-reperfusion injury in vivo.
- Local anesthetics reduce mortality and protect against renal and hepatic dysfunction in murine septic peritonitis.
- Renal failure due to acute nephrocalcinosis following oral sodium phosphate bowel cleansing.
- A1 adenosine receptor knockout mice exhibit increased renal injury following ischemia and reperfusion.
- A1 adenosine receptor activation inhibits inflammation, necrosis, and apoptosis after renal ischemia-reperfusion injury in mice.
- Proliferative glomerulonephritis with monoclonal IgG deposits: a distinct entity mimicking immune-complex glomerulonephritis.
- IgA-dominant acute poststaphylococcal glomerulonephritis complicating diabetic nephropathy.
- A dual pattern of immunofluorescence positivity.
- Toxic acute tubular necrosis following treatment with zoledronate (Zometa).
- Foamy podocytes.
- Granulomatous interstitial nephritis.
- A 14-year-old male with asymptomatic proteinuria and hearing loss.
- A rare infectious cause of renal allograft dysfunction.
- A rare complication of monoclonal gammopathy.
- Idiopathic nodular glomerulosclerosis is a distinct clinicopathologic entity linked to hypertension and smoking.
- Crystalline nephropathy due to 2,8-dihydroxyadeninuria: an under-recognized cause of irreversible renal failure.
- Light chain tubulopathy without Fanconi syndrome.
- Thin basement membrane nephropathy cannot be diagnosed reliably in deparaffinized, formalin-fixed tissue.
- Acute poststaphylococcal glomerulonephritis superimposed on diabetic glomerulosclerosis.
- Methotrexate-associated B-cell lymphoma presenting with acute renal failure and bilateral nephromegaly.
- IgG1 lambda light and heavy chain renal amyloidosis.
- Recurrent hemolytic uremic syndrome in the renal allograft.
- C1q nephropathy: a variant of focal segmental glomerulosclerosis.
- Dysproteinemia, proteinuria, and glomerulonephritis.
- Paraplegia, proteinuria, and renal failure.
- Sickle cell disease, nephrotic syndrome, and renal failure.
- Multiple myeloma, nephrotic syndrome and crystalloid inclusions in podocytes.
- Immunofluorescence on pronase-digested paraffin sections: a valuable salvage technique for renal biopsies.
- Uromodulin storage disease.
- De novo AL amyloidosis in the kidney allograft.
- A destructive nasal lesion and glomerulonephritis.
- Myeloma cast nephropathy, direct renal infiltration by myeloma, and renal extramedullary hematopoiesis.
- Secondary oxalosis due to excess vitamin C intake.
- Nephrotoxicity of antiretroviral therapy in an HIV-infected patient.
- AIDS, nephrotic-range proteinuria, and renal failure.
- Chronic lymphocytic leukemia and cryoglobulinemic glomerulonephritis.
- Chyluria presenting as milky urine and nephrotic-range proteinuria.
- Acute onset of hematuria and proteinuria associated with multiorgan involvement of the heart, liver, pancreas, kidneys, and skin in a patient with Henoch-Schönlein pur...
- Microscopic intrarenal particles after pulsatile machine preservation do not adversely affect outcomes after renal transplantation.
- A single gene for human TRAF-3 at chromosome 14q32.3 encodes a variety of mRNA species by alternative polyadenylation, mRNA splicing and transcription initiation.
- Characterization of an intron 12 splice donor mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Doctors Specialties
- Anatomic Pathology
- Clinical Pathology
- Pathology
Accepted Insurances
- Choice Plus POS II
- Assurant Health
- Blue Card PPO
- Blue Cross Blue Shield of Illinois PPO
- Humana
- Medica
- Medicaid
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Priority Health
- Choice Plus POS
- Options PPO
- United Healthcare
- Wisconsin Physicians Service
Education
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New York Presbyterian Hospital -
Damascus University Faculty of Medicine
Hospital
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Mayo Clinic - Rochester, Minnesota
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1376670679 |
| Last Name Of The Provider | NASR |
| First Name Of The Provider | SAMIH |
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