Craig B Langman
Overview
Explore the profile of Craig B Langman including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
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111
Citations
1925
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Recent Articles
21.
Eisner B, Goldfarb D, Baum M, Langman C, Curhan G, Preminger G, et al.
J Endourol
. 2020 Feb;
34(11):1103-1110.
PMID: 32066273
Cystinuria is a genetic disorder with both autosomal recessive and incompletely dominant inheritance. The disorder disrupts cystine and other dibasic amino acid transport in proximal tubules of the kidney, resulting...
22.
Kasimer R, Langman C
Pediatr Nephrol
. 2020 Feb;
36(2):223-236.
PMID: 32016627
While nephropathic cystinosis is classically thought of as a childhood disease, with improved treatments, patients are more commonly living into adulthood. We performed a systematic review of the literature available...
23.
Onder A, Flynn J, Billings A, Deng F, Defreitas M, Katsoufis C, et al.
Pediatr Nephrol
. 2019 Nov;
35(2):287-295.
PMID: 31696356
Background: Permanent vascular access (PVA) is preferred for long-term hemodialysis. Arteriovenous fistulae (AVF) have the best patency and the lowest complication rates compared to arteriovenous grafts (AVG) and tunneled cuffed...
24.
Langman C
Kidney Int
. 2019 Jul;
96(2):275-277.
PMID: 31331465
Nephropathic cystinosis is the most common genetic cause of a renal Fanconi syndrome and results from dysfunction of the lysosomal cystine-transporter protein cystinosin. The multiple organ dysfunctions of affected patients...
25.
Okuda Y, Obi Y, Streja E, Laster M, Rhee C, Langman C, et al.
Pediatr Nephrol
. 2019 Jun;
34(10):1799-1809.
PMID: 31218394
Background: Hypoalbuminemia is a strong predictor of hospitalization and mortality among adult dialysis patients. However, data are scant on the association between serum albumin and hospitalization among children new to...
26.
Brooks E, Lin D, Langman C, Thompson J, John-Williams L, Furth S, et al.
Kidney Int Rep
. 2019 May;
4(5):720-723.
PMID: 31080927
No abstract available.
27.
Lingeman J, Pareek G, Easter L, Pease R, Grujic D, Brettman L, et al.
Int Urol Nephrol
. 2019 Feb;
51(4):601-608.
PMID: 30783888
Purpose: To evaluate the potential of ALLN-177, an orally administered, oxalate-specific enzyme therapy to reduce urine oxalate (UOx) excretion in patients with secondary hyperoxaluria. Methods: Sixteen male and female subjects...
28.
Onder A, Flynn J, Billings A, Deng F, Defreitas M, Katsoufis C, et al.
Pediatr Nephrol
. 2019 Jan;
34(8):1483-1484.
PMID: 30684015
The original version of this article unfortunately contained a mistake. The name of Vimal Chadha was presented incorrectly. The corrected author list is given above.
29.
Brooks E, Deng F, Weese-Mayer D, Kuntz N, Langman C
Kidney Int Rep
. 2018 Nov;
3(6):1489-1496.
PMID: 30450477
No abstract available.
30.
Laster M, Soohoo M, Streja E, Elashoff R, Jernigan S, Langman C, et al.
Pediatr Nephrol
. 2018 Sep;
34(1):107-115.
PMID: 30267239
Background: Studies in healthy pediatric populations and adults treated with dialysis demonstrate higher parathyroid hormone (PTH) and lower 25-hydroxyvitamin D levels in African-Americans. Despite these findings, African-Americans on dialysis demonstrate...