关注
Christian Hanna
Christian Hanna
Assistant Professor of Pediatrics, Mayo Clinic
在 mayo.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis
A Daga, AJ Majmundar, DA Braun, HY Gee, JA Lawson, S Shril, ...
Kidney international 93 (1), 204-213, 2018
1672018
TGF-β/Smad3 activates mammalian target of rapamycin complex-1 to promote collagen production by increasing HIF-1α expression
B Rozen-Zvi, T Hayashida, SC Hubchak, C Hanna, LC Platanias, ...
American Journal of Physiology-Renal Physiology 305 (4), F485-F494, 2013
782013
IgA nephropathy presenting as macroscopic hematuria in 2 pediatric patients after receiving the Pfizer COVID-19 vaccine
C Hanna, LPH Hernandez, L Bu, S Kizilbash, L Najera, MN Rheault, ...
Kidney international 100 (3), 705-706, 2021
702021
Hypoxia-inducible factor-2α and TGF-β signaling interact to promote normoxic glomerular fibrogenesis
C Hanna, SC Hubchak, X Liang, B Rozen-Zvi, PT Schumacker, ...
American Journal of Physiology-Renal Physiology 305 (9), F1323-F1331, 2013
622013
Quality of life is improved and kidney function preserved in patients with nephropathic cystinosis treated for 2 years with delayed-release cysteamine bitartrate
CB Langman, LA Greenbaum, P Grimm, M Sarwal, P Niaudet, ...
The Journal of pediatrics 165 (3), 528-533. e1, 2014
592014
Outcomes and risk factors for graft loss: lessons learned from 1,056 pediatric kidney transplants at the University of Minnesota
S Chinnakotla, P Verghese, B Chavers, MN Rheault, V Kirchner, T Dunn, ...
Journal of the American College of Surgeons 224 (4), 473-486, 2017
442017
High prevalence of kidney cysts in patients with CYP24A1 deficiency
C Hanna, TA Potretzke, AG Cogal, YG Mkhaimer, PJ Tebben, VE Torres, ...
Kidney International Reports 6 (7), 1895-1903, 2021
122021
Congenital heart disease in adults with autosomal dominant polycystic kidney disease
M Chedid, C Hanna, G Zaatari, Y Mkhaimer, P Reddy, L Rangel, ...
American journal of nephrology 53 (4), 316-324, 2022
92022
Kidney cysts in hypophosphatemic rickets with hypercalciuria: a case series
C Hanna, TA Potretzke, M Chedid, LJ Rangel, J Arroyo, D Zubidat, ...
Kidney Medicine 4 (3), 100419, 2022
82022
Cardiovascular outcomes in kidney transplant recipients with ADPKD
M Chedid, HD Kaidbay, S Wigerinck, Y Mkhaimer, B Smith, D Zubidat, ...
Kidney International Reports 7 (9), 1991-2005, 2022
62022
De novo PBX1 variant in a patient with glaucoma, kidney anomalies, and developmental delay: An expansion of the CAKUTHED phenotype
SL Safgren, RJ Olson, F Pinto e Vairo, ED Bothun, C Hanna, EW Klee, ...
American Journal of Medical Genetics Part A 188 (3), 919-925, 2022
62022
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
LR Claus, C Chen, J Stallworth, JL Turner, GG Slaats, AL Hawks, ...
Kidney International 104 (5), 995-1007, 2023
52023
Cytomegalovirus sinusitis in a child with chronic myelogenous leukemia following bone marrow transplantation
A Rayes, K Sahni, C Hanna, M Suryadevara, P Goyal, I Cherrick
Pediatric blood & cancer 56 (7), 1140-1142, 2011
52011
Bone health in autosomal dominant polycystic kidney disease (ADPKD) patients after kidney transplantation
D Zubidat, C Hanna, AK Randhawa, BH Smith, M Chedid, DHN Kaidbay, ...
Bone Reports 18, 101655, 2023
32023
Asymptomatic pyuria as a prognostic biomarker in autosomal dominant polycystic kidney disease
BE Jones, YG Mkhaimer, LJ Rangel, M Chedid, PJ Schulte, AK Mohamed, ...
Kidney360 3 (3), 465-476, 2022
32022
A toddler with severe hypercalcemia and pyelonephritis: answers
J Wilbanks, J Hillyer, F Hashim, D Sas, C Hanna
Pediatric Nephrology 36, 859-861, 2021
32021
State of the science and ethical considerations for preimplantation genetic testing for monogenic cystic kidney diseases and ciliopathies
WS Thompson, SN Babayev, ML McGowan, AG Kattah, MJ Wick, ...
Journal of the American Society of Nephrology, 10.1681, 2023
22023
Copeptin levels in hospitalized infants and children with suspected vasopressin-dependent disorders: a case series
A Al Nofal, C Hanna, AN Lteif, ST Pittock, JD Schwartz, JE Brumbaugh, ...
Journal of Pediatric Endocrinology and Metabolism 36 (5), 492-499, 2023
22023
Genetic etiologies, diagnosis, and management of neonatal cystic kidney disease
LS Heidenreich, EM Bendel-Stenzel, PC Harris, C Hanna
NeoReviews 23 (3), e175-e188, 2022
22022
Refractory rhabdomyolysis responsive to corticosteroid therapy
M Hammers, F Hashim, C Hanna, A Farris, S Blasick
Baylor University Medical Center Proceedings 34 (2), 314-315, 2021
22021
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