Pesquisa | Biblioteca Virtual em Saúde

1.

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.

Mann, Nina; Braun, Daniela A; Amann, Kassaundra; Tan, Weizhen; Shril, Shirlee; Connaughton, Dervla M; Nakayama, Makiko; Schneider, Ronen; Kitzler, Thomas M; van der Ven, Amelie T; Chen, Jing; Ityel, Hadas; Vivante, Asaf; Majmundar, Amar J; Daga, Ankana; Warejko, Jillian K; Lovric, Svjetlana; Ashraf, Shazia; Jobst-Schwan, Tilman; Widmeier, Eugen; Hugo, Hannah; Mane, Shrikant M; Spaneas, Leslie; Somers, Michael J G; Ferguson, Michael A; Traum, Avram Z; Stein, Deborah R; Baum, Michelle A; Daouk, Ghaleb H; Lifton, Richard P; Manzi, Shannon; Vakili, Khashayar; Kim, Heung Bae; Rodig, Nancy M; Hildebrandt, Friedhelm.

J Am Soc Nephrol; 30(2): 201-215, 2019 02.

Artigo em Inglês | MEDLINE | ID: mdl-30655312

2.

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

van der Ven, Amelie T; Connaughton, Dervla M; Ityel, Hadas; Mann, Nina; Nakayama, Makiko; Chen, Jing; Vivante, Asaf; Hwang, Daw-Yang; Schulz, Julian; Braun, Daniela A; Schmidt, Johanna Magdalena; Schapiro, David; Schneider, Ronen; Warejko, Jillian K; Daga, Ankana; Majmundar, Amar J; Tan, Weizhen; Jobst-Schwan, Tilman; Hermle, Tobias; Widmeier, Eugen; Ashraf, Shazia; Amar, Ali; Hoogstraaten, Charlotte A; Hugo, Hannah; Kitzler, Thomas M; Kause, Franziska; Kolvenbach, Caroline M; Dai, Rufeng; Spaneas, Leslie; Amann, Kassaundra; Stein, Deborah R; Baum, Michelle A; Somers, Michael J G; Rodig, Nancy M; Ferguson, Michael A; Traum, Avram Z; Daouk, Ghaleb H; Bogdanovic, Radovan; Stajic, Natasa; Soliman, Neveen A; Kari, Jameela A; El Desoky, Sherif; Fathy, Hanan M; Milosevic, Danko; Al-Saffar, Muna; Awad, Hazem S; Eid, Loai A; Selvin, Aravind; Senguttuvan, Prabha; Sanna-Cherchi, Simone.

J Am Soc Nephrol; 29(9): 2348-2361, 2018 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-30143558

3.

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.

Daga, Ankana; Majmundar, Amar J; Braun, Daniela A; Gee, Heon Yung; Lawson, Jennifer A; Shril, Shirlee; Jobst-Schwan, Tilman; Vivante, Asaf; Schapiro, David; Tan, Weizhen; Warejko, Jillian K; Widmeier, Eugen; Nelson, Caleb P; Fathy, Hanan M; Gucev, Zoran; Soliman, Neveen A; Hashmi, Seema; Halbritter, Jan; Halty, Margarita; Kari, Jameela A; El-Desoky, Sherif; Ferguson, Michael A; Somers, Michael J G; Traum, Avram Z; Stein, Deborah R; Daouk, Ghaleb H; Rodig, Nancy M; Katz, Avi; Hanna, Christian; Schwaderer, Andrew L; Sayer, John A; Wassner, Ari J; Mane, Shrikant; Lifton, Richard P; Milosevic, Danko; Tasic, Velibor; Baum, Michelle A; Hildebrandt, Friedhelm.

Kidney Int; 93(1): 204-213, 2018 01.

Artigo em Inglês | MEDLINE | ID: mdl-28893421

4.

Bilateral native nephrectomy reduces systemic oxalate level after combined liver-kidney transplant: A case report.

Villani, Vincenzo; Gupta, Neena; Elias, Nahel; Vagefi, Parsia A; Markmann, James F; Paul, Elahna; Traum, Avram Z; Yeh, Heidi.

Pediatr Transplant; 21(3)2017 May.

Artigo em Inglês | MEDLINE | ID: mdl-28261895

5.

Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patients.

Lin, Angela E; Traum, Avram Z; Sahai, Inderneel; Keppler-Noreuil, Kim; Kukolich, Mary K; Adam, Margaret P; Westra, Sjirk J; Arts, Heleen H.

Am J Med Genet A; 161A(11): 2762-76, 2013 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-24123776

6.

A severely immunocompromised child with uncomplicated oseltamivir-resistant 2009 H1N1 pandemic influenza infection.

Hyle, Emily P; Shu, Bo; Lindstrom, Stephen; Klimov, Alexander; Hancock, Kathy; Ferraro, Mary J; Traum, Avram Z; Michelow, Ian C.

Pediatr Transplant; 16(5): E158-61, 2012 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-21429059

7.

Clinical significance of incidentally discovered renal cysts in pediatric patients.

Botwin, Ariel; Phewplung, Teerasak; Wu, Kaiming; Lim, Ruth; Traum, Avram Z; Gee, Michael S.

Abdom Radiol (NY); 44(8): 2835-2840, 2019 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-30972430

8.

Case records of the Massachusetts General Hospital. Case 37-2010. A 16-year-old girl with confusion, anemia, and thrombocytopenia.

Binder, William D; Traum, Avram Z; Makar, Robert S; Colvin, Robert B.

N Engl J Med; 363(24): 2352-61, 2010 Dec 09.

Artigo em Inglês | MEDLINE | ID: mdl-21142538

9.

Urine proteomic profiling to identify biomarkers of steroid resistance in pediatric nephrotic syndrome.

Traum, Avram Z.

Expert Rev Proteomics; 5(5): 715-9, 2008 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-18937561

10.

Outcome of management strategies for BK virus replication in pediatric renal transplant recipients.

Puliyanda, Dechu P; Toyoda, Mieko; Traum, Avram Z; Flores, Francisco X; Jordan, Stanley; Moudgil, Asha; Somers, Michael J G.

Pediatr Transplant; 12(2): 180-6, 2008 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-18307666

11.

The potential for tolerance in pediatric renal transplantation.

Traum, Avram Z; Ko, Dicken Sc; Kawai, Tatsuo.

Curr Opin Organ Transplant; 13(5): 489-94, 2008 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-19060531

12.

Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.

Warejko, Jillian K; Schueler, Markus; Vivante, Asaf; Tan, Weizhen; Daga, Ankana; Lawson, Jennifer A; Braun, Daniela A; Shril, Shirlee; Amann, Kassaundra; Somers, Michael J G; Rodig, Nancy M; Baum, Michelle A; Daouk, Ghaleb; Traum, Avram Z; Kim, Heung Bae; Vakili, Khashayar; Porras, Diego; Lock, James; Rivkin, Michael J; Chaudry, Gulraiz; Smoot, Leslie B; Singh, Michael N; Smith, Edward R; Mane, Shrikant M; Lifton, Richard P; Stein, Deborah R; Ferguson, Michael A; Hildebrandt, Friedhelm.

Hypertension; 71(4): 691-699, 2018 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-29483232

13.

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.

Warejko, Jillian K; Tan, Weizhen; Daga, Ankana; Schapiro, David; Lawson, Jennifer A; Shril, Shirlee; Lovric, Svjetlana; Ashraf, Shazia; Rao, Jia; Hermle, Tobias; Jobst-Schwan, Tilman; Widmeier, Eugen; Majmundar, Amar J; Schneider, Ronen; Gee, Heon Yung; Schmidt, J Magdalena; Vivante, Asaf; van der Ven, Amelie T; Ityel, Hadas; Chen, Jing; Sadowski, Carolin E; Kohl, Stefan; Pabst, Werner L; Nakayama, Makiko; Somers, Michael J G; Rodig, Nancy M; Daouk, Ghaleb; Baum, Michelle; Stein, Deborah R; Ferguson, Michael A; Traum, Avram Z; Soliman, Neveen A; Kari, Jameela A; El Desoky, Sherif; Fathy, Hanan; Zenker, Martin; Bakkaloglu, Sevcan A; Müller, Dominik; Noyan, Aytul; Ozaltin, Fatih; Cadnapaphornchai, Melissa A; Hashmi, Seema; Hopcian, Jeffrey; Kopp, Jeffrey B; Benador, Nadine; Bockenhauer, Detlef; Bogdanovic, Radovan; Stajic, Natasa; Chernin, Gil; Ettenger, Robert.

Clin J Am Soc Nephrol; 13(1): 53-62, 2018 Jan 06.

Artigo em Inglês | MEDLINE | ID: mdl-29127259

14.

Proteomic analysis in pediatric renal disease.

Traum, Avram Z; Schachter, Asher D.

Semin Nephrol; 27(6): 652-7, 2007 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-18061847

15.

Granulomatous interstitial nephritis as a manifestation of Crohn disease.

Colvin, Robert B; Traum, Avram Z; Taheri, Diana; Jafari, Mohsen; Dolatkhah, Shahaboddin.

Arch Pathol Lab Med; 138(1): 125-7, 2014 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-24377821

16.

Urinary proteome profiling to search for biomarkers in steroid-resistant nephrotic syndrome.

Traum, Avram Z; Schachter, Asher D.

Contrib Nephrol; 160: 29-36, 2008.

Artigo em Inglês | MEDLINE | ID: mdl-18401159

17.

Central nervous system lymphoproliferative disorder in pediatric kidney transplant recipients.

Traum, Avram Z; Rodig, Nancy M; Pilichowska, Monika E; Somers, Michael J G.

Pediatr Transplant; 10(4): 505-12, 2006 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-16712612

18.

SELDI-TOF MS of quadruplicate urine and serum samples to evaluate changes related to storage conditions.

Traum, Avram Z; Wells, Meghan P; Aivado, Manuel; Libermann, Towia A; Ramoni, Marco F; Schachter, Asher D.

Proteomics; 6(5): 1676-80, 2006 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-16447157

19.

Urine proteomic profiling of pediatric nephrotic syndrome.

Khurana, Mona; Traum, Avram Z; Aivado, Manuel; Wells, Meghan P; Guerrero, Manuel; Grall, Franck; Libermann, Towia A; Schachter, Asher D.

Pediatr Nephrol; 21(9): 1257-65, 2006 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-16810512

20.

Transplantation proteomics.

Traum, Avram Z; Schachter, Asher D.

Pediatr Transplant; 9(6): 700-11, 2005 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-16269039

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Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.

Bilateral native nephrectomy reduces systemic oxalate level after combined liver-kidney transplant: A case report.

Sensenbrenner syndrome (Cranioectodermal dysplasia): clinical and molecular analyses of 39 patients including two new patients.

A severely immunocompromised child with uncomplicated oseltamivir-resistant 2009 H1N1 pandemic influenza infection.

Clinical significance of incidentally discovered renal cysts in pediatric patients.

Case records of the Massachusetts General Hospital. Case 37-2010. A 16-year-old girl with confusion, anemia, and thrombocytopenia.

Urine proteomic profiling to identify biomarkers of steroid resistance in pediatric nephrotic syndrome.

Outcome of management strategies for BK virus replication in pediatric renal transplant recipients.

The potential for tolerance in pediatric renal transplantation.

Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.

Proteomic analysis in pediatric renal disease.

Granulomatous interstitial nephritis as a manifestation of Crohn disease.

Urinary proteome profiling to search for biomarkers in steroid-resistant nephrotic syndrome.

Central nervous system lymphoproliferative disorder in pediatric kidney transplant recipients.

SELDI-TOF MS of quadruplicate urine and serum samples to evaluate changes related to storage conditions.

Urine proteomic profiling of pediatric nephrotic syndrome.

Transplantation proteomics.