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Showing 1 to 12 of 25 entries
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[Nephronophthisis].

Casopis lekaru ceskych

Gostof R, Půr J, Jandová L.
PMID: 5856260
Cas Lek Cesk. 1965 Nov 05;104(44):1199-206.

No abstract available.

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Gostof R, Půr J, Jandová L. Nefronoftiza. [Nephronophthisis]. Cas Lek Cesk. 1965;104(44):1199-206
Gostof, R., Půr, J., & Jandová, L. (1965). Nefronoftiza. [Nephronophthisis]. Casopis lekaru ceskych, 104(44), 1199-206.
Gostof, R, et al. "Nefronoftiza." [Nephronophthisis]. Casopis lekaru ceskych vol. 104,44 (1965): 1199-206.
Gostof R, Půr J, Jandová L. Nefronoftiza. [Nephronophthisis]. Cas Lek Cesk. 1965 Nov 05;104(44):1199-206. Czech. PMID: 5856260.
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International symposium on hereditary nephropathies. 6-8 October 1986, Heidelberg, Federal Republic of Germany.

Pediatric nephrology (Berlin, Germany)

[No authors listed]
PMID: 2908671
Pediatr Nephrol. 1987 Jul;1(3):383-560.

No abstract available.

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International symposium on hereditary nephropathies. 6-8 October 1986, Heidelberg, Federal Republic of Germany. Pediatr Nephrol. 1987;1(3):383-560
(1987). International symposium on hereditary nephropathies. 6-8 October 1986, Heidelberg, Federal Republic of Germany. Pediatric nephrology (Berlin, Germany), 1(3), 383-560.
"International symposium on hereditary nephropathies. 6-8 October 1986, Heidelberg, Federal Republic of Germany." Pediatric nephrology (Berlin, Germany) vol. 1,3 (1987): 383-560.
International symposium on hereditary nephropathies. 6-8 October 1986, Heidelberg, Federal Republic of Germany. Pediatr Nephrol. 1987 Jul;1(3):383-560. PMID: 2908671.
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Genetic and cellular bases of congenital renal dysfunction. Introductory remarks on Session 1. Structural defects.

Birth defects original article series

Bearn AG.
PMID: 5522788
Birth Defects Orig Artic Ser. 1970 Sep;6(3):8.

No abstract available.

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Bearn AG. Genetic and cellular bases of congenital renal dysfunction. Introductory remarks on Session 1. Structural defects. Birth Defects Orig Artic Ser. 1970;6(3):8
Bearn, A. G. (1970). Genetic and cellular bases of congenital renal dysfunction. Introductory remarks on Session 1. Structural defects. Birth defects original article series, 6(3), 8.
Bearn, A G. "Genetic and cellular bases of congenital renal dysfunction. Introductory remarks on Session 1. Structural defects." Birth defects original article series vol. 6,3 (1970): 8.
Bearn AG. Genetic and cellular bases of congenital renal dysfunction. Introductory remarks on Session 1. Structural defects. Birth Defects Orig Artic Ser. 1970 Sep;6(3):8. PMID: 5522788.
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[Congenital and hereditary nephropathy in children in a 10 year cohort from 3 clinics].

Ceskoslovenska pediatrie

Kluka V, Pavkovceková O, Tischler V, Ignatova MS, Degtjareva EM.
PMID: 6467436
Cesk Pediatr. 1984 May;39(5):284-8.

No abstract available.

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Kluka V, Pavkovceková O, Tischler V, et al. Vrodené a dedicné nefropatie u detí v desat'rocných súboroch troch kliník. [Congenital and hereditary nephropathy in children in a 10 year cohort from 3 clinics]. Cesk Pediatr. 1984;39(5):284-8
Kluka, V., Pavkovceková, O., Tischler, V., Ignatova, M. S., & Degtjareva, E. M. (1984). Vrodené a dedicné nefropatie u detí v desat'rocných súboroch troch kliník. [Congenital and hereditary nephropathy in children in a 10 year cohort from 3 clinics]. Ceskoslovenska pediatrie, 39(5), 284-8.
Kluka, V, et al. "Vrodené a dedicné nefropatie u detí v desat'rocných súboroch troch kliník." [Congenital and hereditary nephropathy in children in a 10 year cohort from 3 clinics]. Ceskoslovenska pediatrie vol. 39,5 (1984): 284-8.
Kluka V, Pavkovceková O, Tischler V, Ignatova MS, Degtjareva EM. Vrodené a dedicné nefropatie u detí v desat'rocných súboroch troch kliník. [Congenital and hereditary nephropathy in children in a 10 year cohort from 3 clinics]. Cesk Pediatr. 1984 May;39(5):284-8. Slovak. PMID: 6467436.
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Genomic approaches to elucidating the pathophysiology of renal diseases.

Zhonghua yi xue za zhi = Chinese medical journal; Free China ed

Rifai A, Dworkin LD, Chen A.
PMID: 11791941
Zhonghua Yi Xue Za Zhi (Taipei). 2001 Oct;64(10):555-62.

The physiological and pathological processes of the kidney as a whole can now be analyzed with a molecular precision at a genomic-scale. Using massively parallel cDNA microarray technology, the mRNA expression of thousands of genes can be quantified simultaneously....

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Rifai A, Dworkin LD, Chen A. Genomic approaches to elucidating the pathophysiology of renal diseases. Zhonghua Yi Xue Za Zhi (Taipei). 2001;64(10):555-62
Rifai, A., Dworkin, L. D., & Chen, A. (2001). Genomic approaches to elucidating the pathophysiology of renal diseases. Zhonghua yi xue za zhi = Chinese medical journal; Free China ed, 64(10), 555-62.
Rifai, A, et al. "Genomic approaches to elucidating the pathophysiology of renal diseases." Zhonghua yi xue za zhi = Chinese medical journal; Free China ed vol. 64,10 (2001): 555-62.
Rifai A, Dworkin LD, Chen A. Genomic approaches to elucidating the pathophysiology of renal diseases. Zhonghua Yi Xue Za Zhi (Taipei). 2001 Oct;64(10):555-62. PMID: 11791941.
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Enhance the diagnosis of hereditary renal diseases in pediatric field in China.

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

Ding J.
PMID: 16514728
Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):28-9.

No abstract available.

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Ding J. Enhance the diagnosis of hereditary renal diseases in pediatric field in China. Beijing Da Xue Xue Bao Yi Xue Ban. 2006;38(1):28-9
Ding, J. (2006). Enhance the diagnosis of hereditary renal diseases in pediatric field in China. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences, 38(1), 28-9.
Ding, Jie. "Enhance the diagnosis of hereditary renal diseases in pediatric field in China." Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences vol. 38,1 (2006): 28-9.
Ding J. Enhance the diagnosis of hereditary renal diseases in pediatric field in China. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):28-9. PMID: 16514728.
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Recent progress in inherited kidney diseases.

Advances in chronic kidney disease

Warnock DG, Freedman BI, Guay-Woodford L, Bleyer AJ.
PMID: 16580608
Adv Chronic Kidney Dis. 2006 Apr;13(2):95. doi: 10.1053/j.ackd.2006.01.015.

No abstract available.

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Warnock DG, Freedman BI, Guay-Woodford L, et al. Recent progress in inherited kidney diseases. Adv Chronic Kidney Dis. 2006;13(2):95doi: 10.1053/j.ackd.2006.01.015.
Warnock, D. G., Freedman, B. I., Guay-Woodford, L., & Bleyer, A. J. (2006). Recent progress in inherited kidney diseases. Advances in chronic kidney disease, 13(2), 95. https://doi.org/10.1053/j.ackd.2006.01.015
Warnock, David G, et al. "Recent progress in inherited kidney diseases." Advances in chronic kidney disease vol. 13,2 (2006): 95. doi: https://doi.org/10.1053/j.ackd.2006.01.015
Warnock DG, Freedman BI, Guay-Woodford L, Bleyer AJ. Recent progress in inherited kidney diseases. Adv Chronic Kidney Dis. 2006 Apr;13(2):95. doi: 10.1053/j.ackd.2006.01.015. PMID: 16580608.
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Network analysis of genes regulated in renal diseases: implications for a molecular-based classification.

BMC bioinformatics

Bhavnani SK, Eichinger F, Martini S, Saxman P, Jagadish HV, Kretzler M.
PMID: 19761573
BMC Bioinformatics. 2009 Sep 17;10:S3. doi: 10.1186/1471-2105-10-S9-S3.

BACKGROUND: Chronic renal diseases are currently classified based on morphological similarities such as whether they produce predominantly inflammatory or non-inflammatory responses. However, such classifications do not reliably predict the course of the disease and its response to therapy. In...

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Bhavnani SK, Eichinger F, Martini S, et al. Network analysis of genes regulated in renal diseases: implications for a molecular-based classification. BMC Bioinformatics. 2009;10:S3doi: 10.1186/1471-2105-10-S9-S3.
Bhavnani, S. K., Eichinger, F., Martini, S., Saxman, P., Jagadish, H. V., & Kretzler, M. (2009). Network analysis of genes regulated in renal diseases: implications for a molecular-based classification. BMC bioinformatics, 10S3. https://doi.org/10.1186/1471-2105-10-S9-S3
Bhavnani, Suresh K, et al. "Network analysis of genes regulated in renal diseases: implications for a molecular-based classification." BMC bioinformatics vol. 10 (2009): S3. doi: https://doi.org/10.1186/1471-2105-10-S9-S3
Bhavnani SK, Eichinger F, Martini S, Saxman P, Jagadish HV, Kretzler M. Network analysis of genes regulated in renal diseases: implications for a molecular-based classification. BMC Bioinformatics. 2009 Sep 17;10:S3. doi: 10.1186/1471-2105-10-S9-S3. PMID: 19761573; PMCID: PMC2745690.
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Genetics and the kidney: promise, potential, and challenges. Introduction.

Seminars in nephrology

Sedor JR, Freedman BI.
PMID: 20347639
Semin Nephrol. 2010 Mar;30(2):99-100. doi: 10.1016/j.semnephrol.2010.01.001.

No abstract available.

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Sedor JR, Freedman BI. Genetics and the kidney: promise, potential, and challenges. Introduction. Semin Nephrol. 2010;30(2):99-100doi: 10.1016/j.semnephrol.2010.01.001.
Sedor, J. R., & Freedman, B. I. (2010). Genetics and the kidney: promise, potential, and challenges. Introduction. Seminars in nephrology, 30(2), 99-100. https://doi.org/10.1016/j.semnephrol.2010.01.001
Sedor, John R, and Freedman, Barry I. "Genetics and the kidney: promise, potential, and challenges. Introduction." Seminars in nephrology vol. 30,2 (2010): 99-100. doi: https://doi.org/10.1016/j.semnephrol.2010.01.001
Sedor JR, Freedman BI. Genetics and the kidney: promise, potential, and challenges. Introduction. Semin Nephrol. 2010 Mar;30(2):99-100. doi: 10.1016/j.semnephrol.2010.01.001. PMID: 20347639; PMCID: PMC2847592.
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Genetic architecture of complex traits predisposing to nephropathy: hypertension.

Seminars in nephrology

Hunt SC.
PMID: 20347644
Semin Nephrol. 2010 Mar;30(2):150-63. doi: 10.1016/j.semnephrol.2010.01.006.

Blood pressure and hypertension have significant genetic underpinnings that may be age-dependent. The age-dependency, significant contributions from environmental factors such as diet and exercise, and inherent moment-to-moment variability complicate the identification of the genes contributing to the development of...

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Hunt SC. Genetic architecture of complex traits predisposing to nephropathy: hypertension. Semin Nephrol. 2010;30(2):150-63doi: 10.1016/j.semnephrol.2010.01.006.
Hunt, S. C. (2010). Genetic architecture of complex traits predisposing to nephropathy: hypertension. Seminars in nephrology, 30(2), 150-63. https://doi.org/10.1016/j.semnephrol.2010.01.006
Hunt, Steven C. "Genetic architecture of complex traits predisposing to nephropathy: hypertension." Seminars in nephrology vol. 30,2 (2010): 150-63. doi: https://doi.org/10.1016/j.semnephrol.2010.01.006
Hunt SC. Genetic architecture of complex traits predisposing to nephropathy: hypertension. Semin Nephrol. 2010 Mar;30(2):150-63. doi: 10.1016/j.semnephrol.2010.01.006. PMID: 20347644; PMCID: PMC2848968.
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[Inherited kidney diseases in children].

Zhonghua er ke za zhi = Chinese journal of pediatrics

Zhu CH, Zhang AH.
PMID: 34645225
Zhonghua Er Ke Za Zhi. 2021 Sep 02;59(9):804-806. doi: 10.3760/cma.j.cn112140-20210719-00600.

No abstract available.

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Zhu CH, Zhang AH. [Inherited kidney diseases in children]. Zhonghua Er Ke Za Zhi. 2021;59(9):804-806doi: 10.3760/cma.j.cn112140-20210719-00600.
Zhu, C. H., & Zhang, A. H. (2021). [Inherited kidney diseases in children]. Zhonghua er ke za zhi = Chinese journal of pediatrics, 59(9), 804-806. https://doi.org/10.3760/cma.j.cn112140-20210719-00600
Zhu, C H, and Zhang, A H. "[Inherited kidney diseases in children]." Zhonghua er ke za zhi = Chinese journal of pediatrics vol. 59,9 (2021): 804-806. doi: https://doi.org/10.3760/cma.j.cn112140-20210719-00600
Zhu CH, Zhang AH. [Inherited kidney diseases in children]. Zhonghua Er Ke Za Zhi. 2021 Sep 02;59(9):804-806. doi: 10.3760/cma.j.cn112140-20210719-00600. Chinese. PMID: 34645225.
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[How can clinicians accurately diagnose hereditary kidney diseases in the genomic era].

Zhonghua er ke za zhi = Chinese journal of pediatrics

Wang F, Ding J.
PMID: 32872708
Zhonghua Er Ke Za Zhi. 2020 Sep 02;58(9):701-704. doi: 10.3760/cma.j.cn112140-20200707-00695.

No abstract available.

Cite
Wang F, Ding J. [How can clinicians accurately diagnose hereditary kidney diseases in the genomic era]. Zhonghua Er Ke Za Zhi. 2020;58(9):701-704doi: 10.3760/cma.j.cn112140-20200707-00695.
Wang, F., & Ding, J. (2020). [How can clinicians accurately diagnose hereditary kidney diseases in the genomic era]. Zhonghua er ke za zhi = Chinese journal of pediatrics, 58(9), 701-704. https://doi.org/10.3760/cma.j.cn112140-20200707-00695
Wang, F, and Ding, J. "[How can clinicians accurately diagnose hereditary kidney diseases in the genomic era]." Zhonghua er ke za zhi = Chinese journal of pediatrics vol. 58,9 (2020): 701-704. doi: https://doi.org/10.3760/cma.j.cn112140-20200707-00695
Wang F, Ding J. [How can clinicians accurately diagnose hereditary kidney diseases in the genomic era]. Zhonghua Er Ke Za Zhi. 2020 Sep 02;58(9):701-704. doi: 10.3760/cma.j.cn112140-20200707-00695. Chinese. PMID: 32872708.
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Showing 1 to 12 of 25 entries