Amateur Cinematography

Por Kaplan, Bernard
Publicado em 1935

Perspectives in psychological theory : essays in honor of Heinz Werner /

Por Kaplan, Bernard, Wapner, Seymour
Publicado em c196

Hydrochlorothiazide-induced tubulointerstitial nephritis in a patient with Dent disease

Por Marsenic, Olivera, Kaplan, Bernard S.
Publicado no NDT Plus (2009)

An expanded syndrome of dRTA with hearing loss, hyperoxaluria and beta2-microglobulinuria

Por Copelovitch, Lawrence, Kaplan, Bernard S.
Publicado no NDT Plus (2010)

Syphilis Control in a State Prison. III. A Centralized Syphilis Control Program for the State Prisons of New York

Por Brightman, I. Jay, Kaplan, Bernard I.
Publicado em 1942

The Course of the Serologic Tests during Therapeutic Malaria in Patients with Syphilis

Por Kaplan, Bernard I., Brightman, I. Jay
Publicado em 1943

Hypertension and proteinuria - the needle in the haystack?: Answers

Por Denburg, Michelle, Surrey, Lea, Pawel, Bruce, Kaplan, Bernard
Publicado no Pediatr Nephrol (2015)

Current treatment of atypical hemolytic uremic syndrome

Por Kaplan, Bernard S., Ruebner, Rebecca L., Spinale, Joann M., Copelovitch, Lawrence
Publicado em 2014

Rapid progression to end-stage renal disease in a child with a sporadic ACTN4 mutation

Por Kakajiwala, Aadil K., Meyers, Kevin E., Bhatti, Tricia, Kaplan, Bernard S.
Publicado no Clin Nephrol Case Stud (2015)

Post-streptococcal glomerulonephritis associated with atypical hemolytic uremic syndrome: to treat or not to treat with eculizumab?

Por Kakajiwala, Aadil, Bhatti, Tricia, Kaplan, Bernard S., Ruebner, Rebecca L., Copelovitch, Lawrence
Publicado no Clin Kidney J (2016)

Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis

Por Barua, Moumita, Shieh, Eric, Schlondorff, Johannes, Genovese, Giulio, Kaplan, Bernard S, Pollak, Martin R
Publicado em 2013

Extracranial Aneurysms in 2 Patients with Autosomal Recessive Polycystic Kidney Disease

Por Elchediak, Daniel S., Cahill, Anne Marie, Furth, Emma E., Kaplan, Bernard S., Hartung, Erum A.
Publicado no Case Rep Nephrol Dial (2017)

Novel Presentations of Congenital Hyperinsulinism due to Mutations in the MODY genes: HNF1A and HNF4A

Por Stanescu, Diana E., Hughes, Nkecha, Kaplan, Bernard, Stanley, Charles A., De León, Diva D.
Publicado em 2012

Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition

Por Richards, Anna, Buddles, Mark R., Donne, Rosemary L., Kaplan, Bernard S., Kirk, Edwin, Venning, Michael C., Tielemans, Christian L., Goodship, Judith A., Goodship, Timothy H. J.
Publicado em 2001

<it>NPHS2 </it>variation in focal and segmental glomerulosclerosis

Por Savige Judy, Jerums George, Kaplan Bernard S, Al-Waheeb Salah, Katz Avi, Falk Ronald J, Appel Gerald B, Uscinski Andrea, Polu Krishna, Needham Alexander, Tonna Stephen J, Harmon Jennifer, Zhang Kang, Curhan Gary C, Pollak Martin R
Publicado em 2008-09-01

NPHS2 variation in focal and segmental glomerulosclerosis

Por Tonna, Stephen J, Needham, Alexander, Polu, Krishna, Uscinski, Andrea, Appel, Gerald B, Falk, Ronald J, Katz, Avi, Al-Waheeb, Salah, Kaplan, Bernard S, Jerums, George, Savige, Judy, Harmon, Jennifer, Zhang, Kang, Curhan, Gary C, Pollak, Martin R
Publicado em 2008

Nature and Recurrence of AVPR2 Mutations in X-linked Nephrogenic Diabetes Insipidus

Por Bichet, Daniel G., Birnbaumer, Mariel, Lonergan, Michèle, Arthus, Marie-Françoise, Rosenthal, Walter, Goodyer, Paul, Nivet, Hubert, Benoit, Stéphane, Giampietro, Philip, Simonetti, Simonetta, Fish, Alfred, Whitley, Chester B., Jaeger, Philippe, Gertner, Joseph, New, Maria, DiBona, Francis J., Kaplan, Bernard S., Robertson, Gary L., Hendy, Geoffrey N., Fujiwara, T. Mary, Morgan, Kenneth
Publicado em 1994

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

Por Frémeaux-Bacchi, Veronique, Miller, Elizabeth C., Liszewski, M. Kathryn, Strain, Lisa, Blouin, Jacques, Brown, Alison L., Moghal, Nadeem, Kaplan, Bernard S., Weiss, Robert A., Lhotta, Karl, Kapur, Gaurav, Mattoo, Tej, Nivet, Hubert, Wong, William, Gie, Sophie, de Ligny, Bruno Hurault, Fischbach, Michel, Gupta, Ritu, Hauhart, Richard, Meunier, Vincent, Loirat, Chantal, Dragon-Durey, Marie-Agnès, Fridman, Wolf H., Janssen, Bert J. C., Goodship, Timothy H. J., Atkinson, John P.
Publicado em 2008

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

Por Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, Czarnecki, Peter G., Lehman, Anna M., Trnka, Peter, Nitschké, Patrick, Bole-Feysot, Christine, Schueler, Markus, Knebelmann, Bertrand, Burtey, Stéphane, Szabó, Attila J., Tory, Kálmán, Leo, Paul J., Gardiner, Brooke, McKenzie, Fiona A., Zankl, Andreas, Brown, Matthew A., Hartley, Jane L., Maher, Eamonn R., Li, Chunmei, Leroux, Michel R., Scambler, Peter J., Zhan, Shing H., Jones, Steven J., Kayserili, Hülya, Tuysuz, Beyhan, Moorani, Khemchand N., Constantinescu, Alexandru, Krantz, Ian D., Kaplan, Bernard S., Shah, Jagesh V., Hurd, Toby W., Doherty, Dan, Katsanis, Nicholas, Duncan, Emma L., Otto, Edgar A., Beales, Philip L., Mitchison, Hannah M., Saunier, Sophie, Hildebrandt, Friedhelm
Publicado em 2013