Saba Shaid (6 results)
- Softcover
Seller: preigu, Osnabrück, Germanypreigu
Contact seller5-star sellerCondition: New
£ 46.95
£ 59.87 shippingShips from Germany to U.S.A.Quantity: 5 available
Taschenbuch. Condition: Neu. Genetics of Nephrotic Syndrome in Pakistani Children | Saba Shaid | Taschenbuch | 156 S. | Englisch | 2019 | LAP LAMBERT Academic Publishing | EAN 9783330029996 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preig…u.
- Softcover
Seller: Revaluation Books, Exeter, United KingdomRevaluation Books
Contact seller5-star sellerCondition: New
£ 101.32
£ 10.00 shippingShips from United Kingdom to U.S.A.Quantity: 1 available
Paperback. Condition: Brand New. 156 pages. 8.66x5.91x0.36 inches. In Stock.
Language: English
Published by LAP LAMBERT Academic Publishing Apr 2019, 2019
- Softcover
- Print on Demand
Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermanyBuchWeltWeit Ludwig Meier e.K.
Contact seller5-star sellerCondition: New
£ 54.53
£ 19.67 shippingShips from Germany to U.S.A.Quantity: 2 available
Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Nephrotic syndrome (NS) is a common pediatric glomerular disease associated with heavy proteinuria. A significant proportion of the steroid resistant nephrotic syndrome (SRNS) patients are known to have genetic causes for developing… this disease. Advances in the field of medical genetics have revealed that podocytes play a central role in the pathogenesis of SRNS. Recent genetic studies on hereditary NS have identified mutations in a number of genes encoding podocyte proteins. The underlying causes of hereditary NS are the presence of defects in the podocyte architecture and function. The diseases causing mutations found in different forms of NS are in the NPHS1, NPHS2, LAMB2, PLCE1, PTPRO, ACTN4, WT1, CD2A, TRPC6 and INF2 genes. However, mutations in the NPHS1 and NPHS2 genes are among the main causes of early-onset and familial SRNS respectively. The aim of this study was to screen the disease causing mutations in the NPHS1 and NPHS2 genes in a Pakistani SRNS cohort. 156 pp. Englisch.
- Softcover
- Print on Demand
Seller: moluna, Greven, Germanymoluna
Contact seller5-star sellerCondition: New
£ 44.63
£ 41.90 shippingShips from Germany to U.S.A.Quantity: Over 20 available
Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Shaid SabaDr. Saba Shaid - Center of Human Genetics and Molecular Medicine,Sindh Institute of Medical Sciences, Sindh Institute of Urology and Transplantation (SIUT), Karachi, Pakistan.Nephrotic syndrom…e (NS) is a common pediatri.
Language: English
Published by LAP LAMBERT Academic Publishing Apr 2019, 2019
- Softcover
- Print on Demand
Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germanybuchversandmimpf2000
Contact seller5-star sellerCondition: New
£ 54.53
£ 51.31 shippingShips from Germany to U.S.A.Quantity: 1 available
Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Nephrotic syndrome (NS) is a common pediatric glomerular disease associated with heavy proteinuria. A significant proportion of the steroid resistant nephrotic syndrome (SRNS) patients are known to have genetic causes for developing thi…s disease. Advances in the field of medical genetics have revealed that podocytes play a central role in the pathogenesis of SRNS. Recent genetic studies on hereditary NS have identified mutations in a number of genes encoding podocyte proteins. The underlying causes of hereditary NS are the presence of defects in the podocyte architecture and function. The diseases causing mutations found in different forms of NS are in the NPHS1, NPHS2, LAMB2, PLCE1, PTPRO, ACTN4, WT1, CD2A, TRPC6 and INF2 genes. However, mutations in the NPHS1 and NPHS2 genes are among the main causes of early-onset and familial SRNS respectively. The aim of this study was to screen the disease causing mutations in the NPHS1 and NPHS2 genes in a Pakistani SRNS cohort.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 156 pp. Englisch.
- Softcover
- Print on Demand
Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
Contact seller5-star sellerCondition: New
£ 55.18
£ 52.38 shippingShips from Germany to U.S.A.Quantity: 1 available
Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Nephrotic syndrome (NS) is a common pediatric glomerular disease associated with heavy proteinuria. A significant proportion of the steroid resistant nephrotic syndrome (SRNS) patients are known to have genetic causes for developing this… disease. Advances in the field of medical genetics have revealed that podocytes play a central role in the pathogenesis of SRNS. Recent genetic studies on hereditary NS have identified mutations in a number of genes encoding podocyte proteins. The underlying causes of hereditary NS are the presence of defects in the podocyte architecture and function. The diseases causing mutations found in different forms of NS are in the NPHS1, NPHS2, LAMB2, PLCE1, PTPRO, ACTN4, WT1, CD2A, TRPC6 and INF2 genes. However, mutations in the NPHS1 and NPHS2 genes are among the main causes of early-onset and familial SRNS respectively. The aim of this study was to screen the disease causing mutations in the NPHS1 and NPHS2 genes in a Pakistani SRNS cohort.
