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Extracellular Oxidative Stress Markers in COVID-19 Patients with Diabetes as Co-Morbidity.
Clin Pract. 2022 Feb 28;12(2):168-176. doi: 10.3390/clinpract12020021.
Clin Pract. 2022.
PMID: 35314591
Free PMC article.
Serum Chromium Levels in Type 2 Diabetic Patients and Its Association with Glycaemic Control.
Rajendran K, Manikandan S, Nair LD, Karuthodiyil R, Vijayarajan N, Gnanasekar R, Kapil VV, Mohamed AS.
Rajendran K, et al.
J Clin Diagn Res. 2015 Nov;9(11):OC05-8. doi: 10.7860/JCDR/2015/16062.6753. Epub 2015 Nov 1.
J Clin Diagn Res. 2015.
PMID: 26676175
Free PMC article.
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Absence of Nails, Deaf-mutism, Seizures, and Intellectual Disability: A Case Report.
Nair LD, Sagayaraj B, Kumar R.
Nair LD, et al.
J Clin Diagn Res. 2015 Apr;9(4):SD01-3. doi: 10.7860/JCDR/2015/12086.5763. Epub 2015 Apr 1.
J Clin Diagn Res. 2015.
PMID: 26023614
Free PMC article.
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Incontinence in Intellectual Disability: An Under Recognized Cause.
Nair LD, Sagayaraj B, V T T R, Kumar R.
Nair LD, et al.
J Clin Diagn Res. 2015 Sep;9(9):SD01-2. doi: 10.7860/JCDR/2015/14019.6448. Epub 2015 Sep 1.
J Clin Diagn Res. 2015.
PMID: 26500975
Free PMC article.
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Epilepsy in KCNH1-related syndromes.
Mastrangelo M, Scheffer IE, Bramswig NC, Nair LD, Myers CT, Dentici ML, Korenke GC, Schoch K, Campeau PM, White SM, Shashi V, Kansagra S, Van Essen AJ, Leuzzi V.
Mastrangelo M, et al.
Epileptic Disord. 2016 Jun 1;18(2):123-36. doi: 10.1684/epd.2016.0830.
Epileptic Disord. 2016.
PMID: 27267311
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Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.
Kortüm F, Caputo V, Bauer CK, Stella L, Ciolfi A, Alawi M, Bocchinfuso G, Flex E, Paolacci S, Dentici ML, Grammatico P, Korenke GC, Leuzzi V, Mowat D, Nair LD, Nguyen TT, Thierry P, White SM, Dallapiccola B, Pizzuti A, Campeau PM, Tartaglia M, Kutsche K.
Kortüm F, et al.
Nat Genet. 2015 Jun;47(6):661-7. doi: 10.1038/ng.3282. Epub 2015 Apr 27.
Nat Genet. 2015.
PMID: 25915598
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DOORS syndrome: phenotype, genotype and comparison with Coffin-Siris syndrome.
Campeau PM, Hennekam RC; DOORS syndrome collaborative group.
Campeau PM, et al.
Am J Med Genet C Semin Med Genet. 2014 Sep;166C(3):327-32. doi: 10.1002/ajmg.c.31412. Epub 2014 Aug 28.
Am J Med Genet C Semin Med Genet. 2014.
PMID: 25169651
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The genetic basis of DOORS syndrome: an exome-sequencing study.
Campeau PM, Kasperaviciute D, Lu JT, Burrage LC, Kim C, Hori M, Powell BR, Stewart F, Félix TM, van den Ende J, Wisniewska M, Kayserili H, Rump P, Nampoothiri S, Aftimos S, Mey A, Nair LD, Begleiter ML, De Bie I, Meenakshi G, Murray ML, Repetto GM, Golabi M, Blair E, Male A, Giuliano F, Kariminejad A, Newman WG, Bhaskar SS, Dickerson JE, Kerr B, Banka S, Giltay JC, Wieczorek D, Tostevin A, Wiszniewska J, Cheung SW, Hennekam RC, Gibbs RA, Lee BH, Sisodiya SM.
Campeau PM, et al.
Lancet Neurol. 2014 Jan;13(1):44-58. doi: 10.1016/S1474-4422(13)70265-5. Epub 2013 Nov 29.
Lancet Neurol. 2014.
PMID: 24291220
Free PMC article.
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