Prevention of pruritus with ethyl-chloride in skin prick test: a double-blind placebo-controlled prospective study

Por Gal-Oz, Amir, Kivity, Shmuel, Shacham, Yacov, Fiszer, Elisheva, Rogowsky, Ori, Chernin, Gil
Publicado no Allergy Asthma Clin Immunol (2015)

Adequate use of allele frequencies in Hispanics—a problem elucidated in nephrotic syndrome

Por Chernin, Gil, Heeringa, Saskia F., Vega-Warner, Virginia, Schoeb, Dominik S., Nürnberg, Peter, Hildebrandt, Friedhelm
Publicado em 2009

Care of undocumented-uninsured immigrants in a large urban dialysis unit

Por Chernin, Gil, Gal-Oz, Amir, Schwartz, Idit F, Shashar, Moshe, Schwartz, Doron, Weinstein, Talia
Publicado em 2012

Anemia and iron deficiency in COPD patients: prevalence and the effects of correction of the anemia with erythropoiesis stimulating agents and intravenous iron

Por Silverberg, Donald S, Mor, Ram, Weu, Melanie Tia, Schwartz, Doron, Schwartz, Idit F, Chernin, Gil
Publicado em 2014

When the chimney is blocked: malignant renovascular hypertension after endovascular repair of abdominal aortic aneurysm

Por Gal-Oz, Amir, Wolf, Yehuda G, Rosen, Galia, Sharon, Haggai, Schwartz, Idit F, Chernin, Gil
Publicado em 2013

Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Por Chernin, Gil, Vega-Warner, Virginia, Schoeb, Dominik S., Heeringa, Saskia F., Ovunc, Bugsu, Saisawat, Pawaree, Cleper, Roxana, Ozaltin, Fatih, Hildebrandt, Friedhelm
Publicado em 2010

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Por Heeringa, Saskia F., Vlangos, Christopher N., Chernin, Gil, Hinkes, Bernward, Gbadegesin, Rasheed, Liu, Jinhong, Hoskins, Bethan E., Ozaltin, Fatih, Hildebrandt, Friedhelm
Publicado em 2008

Target Hemoglobin May Be Achieved with Intravenous Iron Alone in Anemic Patients with Cardiorenal Syndrome: An Observational Study

Por Ben-Assa, Eyal, Shacham, Yacov, Shashar, Moshe, Leshem-Rubinow, Eran, Gal-Oz, Amir, Schwartz, Idit F., Schwartz, Doron, Silverberg, Donald S., Chernin, Gil
Publicado no Cardiorenal Med (2015)

A Novel TRPC6 Mutation That Causes Childhood FSGS

Por Heeringa, Saskia F., Möller, Clemens C., Du, Jianyang, Yue, Lixia, Hinkes, Bernward, Chernin, Gil, Vlangos, Christopher N., Hoyer, Peter F., Reiser, Jochen, Hildebrandt, Friedhelm
Publicado em 2009

Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria

Por Ovunc, Bugsu, Otto, Edgar A., Vega-Warner, Virginia, Saisawat, Pawaree, Ashraf, Shazia, Ramaswami, Gokul, Fathy, Hanan M., Schoeb, Dominik, Chernin, Gil, Lyons, Robert H., Yilmaz, Engin, Hildebrandt, Friedhelm
Publicado em 2011

Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)

Por Schoeb, Dominik S., Chernin, Gil, Heeringa, Saskia F., Matejas, Verena, Held, Susanne, Vega-Warner, Virginia, Bockenhauer, Detlef, Vlangos, Christopher N., Moorani, Khemchand N., Neuhaus, Thomas J., Kari, Jameela A., MacDonald, James, Saisawat, Pawaree, Ashraf, Shazia, Ovunc, Bugsu, Zenker, Martin, Hildebrandt, Friedhelm
Publicado em 2010

The Phosphate Binder Ferric Citrate and Mineral Metabolism and Inflammatory Markers in Maintenance Dialysis Patients: Results From Prespecified Analyses of a Randomized Clinical Tr...

Por Van Buren, Peter N., Lewis, Julia B., Dwyer, Jamie P., Greene, Tom, Middleton, John, Sika, Mohammed, Umanath, Kausik, Abraham, Josephine D., Arfeen, Shahabul S., Bowline, Isai G., Chernin, Gil, Fadem, Stephen Z., Goral, Simin, Koury, Mark, Sinsakul, Marvin V., Weiner, Daniel E.
Publicado no Am J Kidney Dis (2015)

Screening for NPHS2 Mutations May Help Predict FSGS Recurrence after Transplantation

Por Jungraithmayr, Therese C., Hofer, Katrin, Cochat, Pierre, Chernin, Gil, Cortina, Gerard, Fargue, Sonja, Grimm, Paul, Knueppel, Tanja, Kowarsch, Andreas, Neuhaus, Thomas, Pagel, Philipp, Pfeiffer, Karl P., Schäfer, Franz, Schönermarck, Ulf, Seeman, Tomas, Toenshoff, Burkhard, Weber, Stefanie, Winn, Michelle P., Zschocke, Johannes, Zimmerhackl, Lothar B.
Publicado em 2011

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

Por Hildebrandt, Friedhelm, Heeringa, Saskia F., Rüschendorf, Franz, Attanasio, Massimo, Nürnberg, Gudrun, Becker, Christian, Seelow, Dominik, Huebner, Norbert, Chernin, Gil, Vlangos, Christopher N., Zhou, Weibin, O'Toole, John F., Hoskins, Bethan E., Wolf, Matthias T. F., Hinkes, Bernward G., Chaib, Hassan, Ashraf, Shazia, Schoeb, Dominik S., Ovunc, Bugsu, Allen, Susan J., Vega-Warner, Virginia, Wise, Eric, Harville, Heather M., Lyons, Robert H., Washburn, Joseph, MacDonald, James, Nürnberg, Peter, Otto, Edgar A.
Publicado em 2009

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling

Por Gee, Heon Yung, Saisawat, Pawaree, Ashraf, Shazia, Hurd, Toby W., Vega-Warner, Virginia, Fang, Humphrey, Beck, Bodo B., Gribouval, Olivier, Zhou, Weibin, Diaz, Katrina A., Natarajan, Sivakumar, Wiggins, Roger C., Lovric, Svjetlana, Chernin, Gil, Schoeb, Dominik S., Ovunc, Bugsu, Frishberg, Yaacov, Soliman, Neveen A., Fathy, Hanan M., Goebel, Heike, Hoefele, Julia, Weber, Lutz T., Innis, Jeffrey W., Faul, Christian, Han, Zhe, Washburn, Joseph, Antignac, Corinne, Levy, Shawn, Otto, Edgar A., Hildebrandt, Friedhelm
Publicado em 2013

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Por Heeringa, Saskia F., Chernin, Gil, Chaki, Moumita, Zhou, Weibin, Sloan, Alexis J., Ji, Ziming, Xie, Letian X., Salviati, Leonardo, Hurd, Toby W., Vega-Warner, Virginia, Killen, Paul D., Raphael, Yehoash, Ashraf, Shazia, Ovunc, Bugsu, Schoeb, Dominik S., McLaughlin, Heather M., Airik, Rannar, Vlangos, Christopher N., Gbadegesin, Rasheed, Hinkes, Bernward, Saisawat, Pawaree, Trevisson, Eva, Doimo, Mara, Casarin, Alberto, Pertegato, Vanessa, Giorgi, Gianpietro, Prokisch, Holger, Rötig, Agnès, Nürnberg, Gudrun, Becker, Christian, Wang, Su, Ozaltin, Fatih, Topaloglu, Rezan, Bakkaloglu, Aysin, Bakkaloglu, Sevcan A., Müller, Dominik, Beissert, Antje, Mir, Sevgi, Berdeli, Afig, ϖzen, Seza, Zenker, Martin, Matejas, Verena, Santos-Ocaña, Carlos, Navas, Placido, Kusakabe, Takehiro, Kispert, Andreas, Akman, Sema, Soliman, Neveen A., Krick, Stefanie, Mundel, Peter, Reiser, Jochen, Nürnberg, Peter, Clarke, Catherine F., Wiggins, Roger C., Faul, Christian, Hildebrandt, Friedhelm
Publicado em 2011

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

Por O’Toole, John F., Liu, Yangjian, Davis, Erica E., Westlake, Christopher J., Attanasio, Massimo, Otto, Edgar A., Seelow, Dominik, Nurnberg, Gudrun, Becker, Christian, Nuutinen, Matti, Kärppä, Mikko, Ignatius, Jaakko, Uusimaa, Johanna, Pakanen, Salla, Jaakkola, Elisa, van den Heuvel, Lambertus P., Fehrenbach, Henry, Wiggins, Roger, Goyal, Meera, Zhou, Weibin, Wolf, Matthias T.F., Wise, Eric, Helou, Juliana, Allen, Susan J., Murga-Zamalloa, Carlos A., Ashraf, Shazia, Chaki, Moumita, Heeringa, Saskia, Chernin, Gil, Hoskins, Bethan E., Chaib, Hassan, Gleeson, Joseph, Kusakabe, Takehiro, Suzuki, Takako, Isaac, R. Elwyn, Quarmby, Lynne M., Tennant, Bryan, Fujioka, Hisashi, Tuominen, Hannu, Hassinen, Ilmo, Lohi, Hellevi, van Houten, Judith L., Rotig, Agnes, Sayer, John A., Rolinski, Boris, Freisinger, Peter, Madhavan, Sethu M., Herzer, Martina, Madignier, Florence, Prokisch, Holger, Nurnberg, Peter, Jackson, Peter K., Khanna, Hemant, Katsanis, Nicholas, Hildebrandt, Friedhelm
Publicado em 2010

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

Por O’Toole, John F., Liu, Yangjian, Davis, Erica E., Westlake, Christopher J., Attanasio, Massimo, Otto, Edgar A., Seelow, Dominik, Nurnberg, Gudrun, Becker, Christian, Nuutinen, Matti, Kärppä, Mikko, Ignatius, Jaakko, Uusimaa, Johanna, Pakanen, Salla, Jaakkola, Elisa, van den Heuvel, Lambertus P., Fehrenbach, Henry, Wiggins, Roger, Goyal, Meera, Zhou, Weibin, Wolf, Matthias T.F., Wise, Eric, Helou, Juliana, Allen, Susan J., Murga-Zamalloa, Carlos A., Ashraf, Shazia, Chaki, Moumita, Heeringa, Saskia, Chernin, Gil, Hoskins, Bethan E., Chaib, Hassan, Gleeson, Joseph, Kusakabe, Takehiro, Suzuki, Takako, Isaac, R. Elwyn, Quarmby, Lynne M., Tennant, Bryan, Fujioka, Hisashi, Tuominen, Hannu, Hassinen, Ilmo, Lohi, Hellevi, van Houten, Judith L., Rotig, Agnes, Sayer, John A., Rolinski, Boris, Freisinger, Peter, Madhavan, Sethu M., Herzer, Martina, Madignier, Florence, Prokisch, Holger, Nurnberg, Peter, Jackson, Peter, Khanna, Hemant, Katsanis, Nicholas, Hildebrandt, Friedhelm
Publicado em 2010