Որոնման արդյունքները - Joy Bryant
- Ցուցադրվում են 1 - 10 արդյունքները 10
-
1
Hepatorenal findings in obligate heterozygotes for autosomal recessive polycystic kidney disease Meral Gunay‐Aygun, Baris I. Turkbey, Joy Bryant, Kailash T. Daryanani, Maya T. Gerstein, Katie Piwnica–Worms, Peter L. Choyke, Theo Heller, William A. Gahl
Հրապարակվել է 2011Artigo -
2
Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) Barış Türkbey, İclal Ocak, Kailash Daryanani, Esperanza Font–Montgomery, Linda Lukose, Joy Bryant, M. Tuchman, Parvathi Mohan, Theo Heller, William A. Gahl, Peter L. Choyke, Meral Gunay‐Aygun
Հրապարակվել է 2008Revisão -
3
A 3-year randomized therapeutic trial of nitisinone in alkaptonuria Wendy J. Introne, Monique B. Perry, James Troendle, Ekaterini Tsilou, Michael A. Kayser, Pim Suwannarat, Kevin E. O'Brien, Joy Bryant, Vandana Sachdev, James C. Reynolds, Elizabeth Moylan, Isa Bernardini, William A. Gahl
Հրապարակվել է 2011Artigo -
4
Comprehensive Endocrine-Metabolic Evaluation of Patients With Alström Syndrome Compared With BMI-Matched Controls Joan C. Han, Daniela P. Reyes-Capó, Chia‐Ying Liu, James C. Reynolds, Evrim Türkbey, Barış Türkbey, Joy Bryant, Jan D. Marshall, Jürgen Κ. Naggert, William A. Gahl, Jack A. Yanovski, Meral Gunay‐Aygun
Հրապարակվել է 2018Artigo -
5
PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis Meral Gunay‐Aygun, M. Tuchman, Esperanza Font–Montgomery, Linda Lukose, Hailey Edwards, Angelica Garcia, Surasawadee Ausavarat, Shira G. Ziegler, Katie Piwnica–Worms, Joy Bryant, Isa Bernardini, Roxanne Fischer, Marjan Huizing, Lisa M. Guay‐Woodford, William A. Gahl
Հրապարակվել է 2009Artigo -
6
Prospective Evaluation of Kidney Disease in Joubert Syndrome Leah R. Fleming, Daniel Doherty, Melissa A. Parisi, Ian Glass, Joy Bryant, Roxanne Fischer, Barış Türkbey, Peter L. Choyke, Kailash Daryanani, Meghana Vemulapalli, James C. Mullikin, May Christine V. Malicdan, Thierry Vilboux, John A. Sayer, William A. Gahl, Meral Gunay‐Aygun
Հրապարակվել է 2017Artigo -
7
Mutations in human homologue of chicken<i>talpid3</i>gene (<i>KIAA0586</i>) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes May Christine V. Malicdan, Thierry Vilboux, Joshi Stephen, Dino Maglic, Luhe Mian, Daniel Konzman, Jennifer Guo, Deniz Yildirimli, Joy Bryant, Roxanne Fischer, Wadih M. Zein, Joseph Snow, Meghana Vemulapalli, James C. Mullikin, Camilo Toro, Benjamin D. Solomon, John E. Niederhuber, William A. Gahl, Meral Gunay‐Aygun
Հրապարակվել է 2015Artigo -
8
Characteristics of Congenital Hepatic Fibrosis in a Large Cohort of Patients With Autosomal Recessive Polycystic Kidney Disease Meral Gunay‐Aygun, Esperanza Font–Montgomery, Linda Lukose, Maya T. Gerstein, Katie Piwnica–Worms, Peter L. Choyke, Kailash T. Daryanani, Barış Türkbey, Roxanne Fischer, Isa Bernardini, Murat Sincan, Xiongce Zhao, Netanya G. Sandler, Annelys Roque, Daniel C. Douek, Jennifer Graf, Marjan Huizing, Joy Bryant, Parvathi Mohan, William A. Gahl, Theo Heller
Հրապարակվել է 2012Artigo -
9
Correlation of Kidney Function, Volume and Imaging Findings, and PKHD1 Mutations in 73 Patients with Autosomal Recessive Polycystic Kidney Disease Meral Gunay‐Aygun, Esperanza Font–Montgomery, Linda Lukose, M. Tuchman, Jennifer Graf, Joy Bryant, Robert Kleta, Angelica Garcia, Hailey Edwards, Katie Piwnica–Worms, David H. Adams, Isa Bernardini, Roxanne Fischer, Donna M. Krasnewich, Neal L. Oden, Alexander Ling, Zenaide Quezado, Colleen Zak, Kailash T. Daryanani, Barış Türkbey, Peter L. Choyke, Lisa M. Guay‐Woodford, William A. Gahl
Հրապարակվել է 2010Artigo -
10
Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI) Carlos R. Ferreira, Mary E. Hackbarth, Shira G. Ziegler, Kristen S. Pan, Mary Scott Roberts, Douglas R. Rosing, Margaret Whelpley, Joy Bryant, Ellen F. Macnamara, Sisi Wang, Kerstin Müller, Iris R. Hartley, Emily Y. Chew, Timothy E. Corden, Christina M. Jacobsen, Ingrid A. Holm, Frank Rutsch, Esra Dikoglu, Marcus Y. Chen, M. Zulf Mughal, Michael A. Levine, Rachel I. Gafni, William A. Gahl
Հրապարակվել է 2020Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Internal medicine
Medicine
Autosomal Recessive Polycystic Kidney Disease
Pathology
Polycystic kidney disease
Biology
Gene
Kidney
Phenotype
Gastroenterology
Genetics
Cirrhosis
Congenital hepatic fibrosis
Kidney disease
Mutation
Nephrology
Nephronophthisis
Portal hypertension
Biochemistry
Chemistry
Ciliopathies
Ciliopathy
Cilium
Compound heterozygosity
Disease
Joubert syndrome
Radiology
Adverse effect
Alkaptonuria
Bioinformatics