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An open-label study to elucidate the effects of standardized Bacopa monnieri extract in the management of symptoms of attention-deficit hyperactivity disorder in children.
Dave UP, Dingankar SR, Saxena VS, Joseph JA, Bethapudi B, Agarwal A, Kudiganti V. Dave UP, et al. Adv Mind Body Med. 2014 Spring;28(2):10-5. Adv Mind Body Med. 2014. PMID: 24682000 Clinical Trial.
Evaluation of BR-16 A (Mentat) in cognitive and behavioural dysfunction of mentally retarded children--a placebo-controlled study.
Dave UP, Chauvan V, Dalvi J. Dave UP, et al. Indian J Pediatr. 1993 May-Jun;60(3):423-8. doi: 10.1007/BF02751207. Indian J Pediatr. 1993. PMID: 8253492 Clinical Trial.
A community genetics approach to population screening in India for mental retardation--a model for developing countries.
Dave U, Shetty N, Mehta L. Dave U, et al. Ann Hum Biol. 2005 Mar-Apr;32(2):195-203. doi: 10.1080/03014460500075381. Ann Hum Biol. 2005. PMID: 16096217
Plasma chitotriosidase activity in children with lysosomal storage disorders.
Sheth JJ, Sheth FJ, Oza NJ, Gambhir PS, Dave UP, Shah RC. Sheth JJ, et al. Among authors: dave up. Indian J Pediatr. 2010 Feb;77(2):203-5. doi: 10.1007/s12098-009-0249-0. Indian J Pediatr. 2010. PMID: 19936666
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease.
Ankleshwaria C, Mistri M, Bavdekar A, Muranjan M, Dave U, Tamhankar P, Khanna V, Jasinge E, Nampoothiri S, Edayankara Kadangot S, Sheth F, Gupta S, Sheth J. Ankleshwaria C, et al. J Hum Genet. 2014 Apr;59(4):223-8. doi: 10.1038/jhg.2014.5. Epub 2014 Feb 13. J Hum Genet. 2014. PMID: 24522292
Novel mutations in the glucocerebrosidase gene of Indian patients with Gaucher disease.
Ankleshwaria C, Mistri M, Bavdekar A, Muranjan M, Dave U, Tamhankar P, Khanna V, Jasinge E, Nampoothiri S, Edayankara Kadangot S, Sheth F, Gupta S, Sheth J. Ankleshwaria C, et al. J Hum Genet. 2015 May;60(5):285. doi: 10.1038/jhg.2015.27. J Hum Genet. 2015. PMID: 26008600 No abstract available.
Cornelia de Lange syndrome in diverse populations.
Dowsett L, Porras AR, Kruszka P, Davis B, Hu T, Honey E, Badoe E, Thong MK, Leon E, Girisha KM, Shukla A, Nayak SS, Shotelersuk V, Megarbane A, Phadke S, Sirisena ND, Dissanayake VHW, Ferreira CR, Kisling MS, Tanpaiboon P, Uwineza A, Mutesa L, Tekendo-Ngongang C, Wonkam A, Fieggen K, Batista LC, Moretti-Ferreira D, Stevenson RE, Prijoles EJ, Everman D, Clarkson K, Worthington J, Kimonis V, Hisama F, Crowe C, Wong P, Johnson K, Clark RD, Bird L, Masser-Frye D, McDonald M, Willems P, Roeder E, Saitta S, Anyane-Yeoba K, Demmer L, Hamajima N, Stark Z, Gillies G, Hudgins L, Dave U, Shalev S, Siu V, Ades A, Dubbs H, Raible S, Kaur M, Salzano E, Jackson L, Deardorff M, Kline A, Summar M, Muenke M, Linguraru MG, Krantz ID. Dowsett L, et al. Am J Med Genet A. 2019 Feb;179(2):150-158. doi: 10.1002/ajmg.a.61033. Epub 2019 Jan 6. Am J Med Genet A. 2019. PMID: 30614194 Free PMC article.
Mutational Screening and Prenatal Diagnosis in Cornelia de Lange syndrome.
Dave U, Shetty D. Dave U, et al. J Obstet Gynaecol India. 2014 Feb;64(1):27-31. doi: 10.1007/s13224-013-0450-y. Epub 2013 Sep 29. J Obstet Gynaecol India. 2014. PMID: 24587603 Free PMC article.
Brain tumours in childhood in Bombay: I: Histopathology showing changing patterns; II: Tissue culture with light and electronmicroscopy, stressing ingestion & degradation of bacteria by glial cells in vitro.
Dastur DK, Kankonkar SR, Manghani DK, Vakil TH, Dave UP, Bhagwati SN. Dastur DK, et al. Among authors: dave up. J Neurooncol. 1989 Jul;7(2):153-64. doi: 10.1007/BF00165100. J Neurooncol. 1989. PMID: 2674339
Clinical and Mutational Characterizations of Ten Indian Patients with Beta-Ketothiolase Deficiency.
Abdelkreem E, Akella RRD, Dave U, Sane S, Otsuka H, Sasai H, Aoyama Y, Nakama M, Ohnishi H, Mahmoud S, Abd El Aal M, Fukao T. Abdelkreem E, et al. JIMD Rep. 2017;35:59-65. doi: 10.1007/8904_2016_26. Epub 2016 Dec 8. JIMD Rep. 2017. PMID: 27928777 Free PMC article.
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