Hereditary kidney diseases /
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| Imprint: | Basel ; New York : Karger, c1997. |
|---|---|
| Description: | xii, 217 p. : ill. ; 25 cm. |
| Language: | English |
| Series: | Contributions to nephrology ; vol. 122 Contributions to nephrology ; v. 122. |
| Subject: | |
| Format: | Print Book |
| URL for this record: | http://pi.lib.uchicago.edu/1001/cat/bib/5998493 |
MARC
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| 049 | |a CGUA | ||
| 050 | 0 | 0 | |a RC903 |b .H47 1997 |
| 060 | 0 | 0 | |a W1 |b CO778UN v.122 1997 |
| 060 | 1 | 0 | |a WJ 300 |b H542 1997 |
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| 245 | 0 | 0 | |a Hereditary kidney diseases / |c volume editors, A. Sessa ... [et al.]. |
| 260 | |a Basel ; |a New York : |b Karger, |c c1997. | ||
| 300 | |a xii, 217 p. : |b ill. ; |c 25 cm. | ||
| 336 | |a text |b txt |2 rdacontent |0 http://id.loc.gov/vocabulary/contentTypes/txt | ||
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| 490 | 1 | |a Contributions to nephrology ; |v vol. 122 | |
| 500 | |a "Vimercate (Milan), Italy, September 28, 1996." | ||
| 504 | |a Includes bibliographical references and indexes. | ||
| 505 | 0 | 0 | |t Pathogenesis of Autosomal Dominant Polycystic Kidney Disease: Recent Developments / |r J. J. Grantham -- |t Autosomal Recessive Polycystic Kidney Disease / |r K. Zerres, J. Becker and G. Mucher -- |t Prevalence of Hypertension According to Phenotype and Gender in Autosomal-Dominant Polycystic Kidney Disease / |r R. Boulahrouz, P. Mazeau and C. Charasse -- |t Role of Renin-Angiotensin-Aldosterone System and of Sympathetic Activity in Arterial Hypertension Associated with Autosomal Dominant Polycystic Kidney Disease / |r G. Cerasola, M. Li Vecchi and G. Mule -- |t Hypertension of Polycystic Kidney Disease Types 1 and 2 and Its Effect on the Age of Onset of End-Stage Renal Disease / |r R. Torra, C. Badenas and L. Perez -- |t Sodium-Lithium Countertransport in Autosomal Polycystic Kidney Disease / |r M. Li Vecchi, G. Andronico and L. Ferrara -- |t Inflammatory Cytokine Profile in Autosomal Dominant Polycystic Kidney Disease / |r M. Merta, V. Tesar and T. Zima -- |t Extracellular Matrix Abnormality May be Responsible for Cyst Development / |r G. Bellinghieri, L. Magaudda and D. Santoro -- |t Mutations and Intragenic Polymorphisms in the Diagnosis of Autosomal Dominant Polycystic Kidney Disease Type 1 / |r C. Badenas, R. Torra and A. Darnell -- |t Expression of Protein Fragments from the Human PKD1 Gene and Production of Rabbit Polyclonal Antibodies to the Recombinant Proteins / |r G. L. Aguiari, A. Bozza and R. Piva -- |t Molecular Genetic Investigations in Autosomal Dominant Polycystic Kidney Disease. Gene Mutation Detection, Linkage Analysis, and Preliminary ACE Gene I/D Polymorphism Association Studies: An Update / |r A. E. Turco, E. Bresin and S. Rossetti -- |t Oral-Facial-Digital Syndrome Type 1 Coexisting with Polycystic Kidney Disease / |r F. Scolari, B. Valzorio and O. Carli -- |t Nephronophthisis-Medullary Cystic Kidney Disease Complex: A Report on 24 Patients from 5 Families with Italian Ancestry / |r F. Scolari, B. Valzorio and V. Vizzardi -- |t Renal Manifestations of Tuberous Sclerosis Complex / |r V. E. Torres, H. Zincke and B. K. King -- |t The TSC2/PKD 1 Contiguous Gene Syndrome / |r P. C. Harris -- |t A Case of Pringle-Bourneville Tuberous Sclerosis with Renal Angiomyolipomas: Clinical and Radiological Aspects / |r F. Cavatorta, S. Campisi and A. Zollo -- |t Tuberous Sclerosis and Nephrocalcinosis / |r F. Schillinger and R. Montagnac -- |t A Tuberous Sclerosis Patient with a Large TSC2 and PKD1 Gene Deletion Shows Extrarenal Signs of Autosomal Dominant Polycystic Disease / |r L. Longa, A. Brusco and C. Carbonara -- |t Tuberous Sclerosis Complex and Early-Onset Autosomal Dominant Polycystic Kidney Disease as a 'Contiguous Gene' Syndrome: Report of a Case / |r C. Mancino and A. Balducci -- |t Pulmonary Lymphangioleiomyomatosis and Tuberous Sclerosis Complex / |r I. Peccatori, F. Pitingolo and G. Battini -- |t The Kidney and Von Hippel-Lindau Disease: Impact of Molecular Genetic Analysis of the VHL Gene for Clinical Management / |r H. P. H. Neumann, B. U. Bender and W. Schultze-Seemann -- |t Von Hippel-Lindau (VHL) Gene Analysis in Italian Families with VHL Disease / |r M. Montera, E. Bellone and F. Ajmar -- |t Planning Kidney Surgery in Von Hippel-Lindau Disease / |r P. Riegler, R. Corradini and W. Passler -- |t Alport Syndrome: Clinical and Genetic Correlation in a Type-IV Collagen Disease / |r K.-O. Netzer, O. Gross and C. Jung -- |t Clinical and Molecular Diagnosis in Inherited Kidney Diseases: Three Examples / |r J.-P. Grunfeld, P. Lesavre and S. Richard -- |t Expression of [alpha](IV) Chains in Alrport's Syndrome and its Correlation with Ultrastructural and Genetic Data / |r G. Mazzucco, P. Barsotti and A. Onetti Muda -- |t Molecular Diagnosis of Alport Syndrome: The Experience in Siena / |r A. Renieri, M. Bruttini and M. Piccini -- |t X-Linked Alport Syndrome with Normal Distribution of Collagen IV [alpha] Chains in Epidermal Basement Membrane / |r I. Naito, S. Nomura and S. Inoue -- |t Kidney Transplantation in Alport's Syndrome / |r F. Scolari, B. Valzorio and F. Fasciolo -- |t Primary Hyperoxaluria / |r R. W. E. Watts -- |t Renal Pathology in Hyperoxaluria / |r A. Onetti Muda, P. Barsotti and S. Rinaldi -- |t Clinical Aspects of Cystinuria / |r A. M. Pierides and C. C. Deltas -- |t Cystinuria: Recent Advances in Pathophysiology and Genetics / |r M. Bruno and M. Marangella -- |t Kidney Involvement in Anderson-Fabry Disease / |r M. Meroni, A. Sessa and G. Battini -- |t Anderson-Fabry Disease. Three Families Detected in Two Years: Unusual Occurrence or Good Interdisciplinary Collaboration? / |r F. Martinelli, F. Bergesio and R. Piperno -- |t Genetic Approach to the Study of Cellular Ion Transport Anomalies in Idiopathic Calcium Nephrolithiasis / |r G. Gambaro, F. Marchini and A. Budakovic -- |t Constitutive Nitric Oxide Synthase Gene Expression in Bartter's and Gitelman's Syndrome and Its Relationship to Their Vascular Hyporesponsiveness / |r L. Calo, M. C. Bordin and P. A. Davis -- |t Familial Hemolytic Uremic Syndrome: Stimulation Linkage Analysis / |r L. Carreras, V. Volpini and R. Poveda -- |t Abnormal Blood Glucose and Insulin Response during Oral Glucose Tolerance Test in Familial Renal Glycosuria / |r S. De Marchi, E. Cecchin and F. Zanello -- |t Renal Transplantation in Patients with Hereditary Kidney Disease: Our Experience / |r V. Mazzarella, G. Splendiani and C. Tozzo -- |t An Information Center for Rare Diseases: A Tool for Epidemiologic and Clinical Studies in Rare Diseases / |r E. Daina, B. Vasile and F. Fiacco. |
| 650 | 0 | |a Kidneys |x Diseases |x Genetic aspects |v Congresses. | |
| 650 | 1 | 2 | |a Kidney Diseases |x genetics |v Congresses. |
| 650 | 7 | |a Kidneys |x Diseases |x Genetic aspects. |2 fast |0 http://id.worldcat.org/fast/fst00987398 | |
| 655 | 7 | |a Conference papers and proceedings. |2 fast |0 http://id.worldcat.org/fast/fst01423772 | |
| 700 | 1 | |a Sessa, A. |0 http://id.loc.gov/authorities/names/n89123960 |1 http://viaf.org/viaf/22184742 | |
| 830 | 0 | |a Contributions to nephrology ; |v v. 122. | |
| 901 | |a ToCBNA |a Analytic | ||
| 903 | |a HeVa | ||
| 903 | |a Hathi | ||
| 929 | |a cat | ||
| 999 | f | f | |i 6f539aae-00fd-5d74-b36d-4000b86866d1 |s c6d0218c-5b59-5744-8650-f782a38f1e55 |
| 928 | |t Library of Congress classification |a RC902.A1C6 v.122 |l ASR |c ASR-SciASR |i 6533695 | ||
| 927 | |t Library of Congress classification |a RC902.A1C6 v.122 |l ASR |c ASR-SciASR |g Analytic |e CRERAR |b A45121764 |i 8019506 | ||
