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Year Number of Results
1985 2
1995 1
1996 2
1998 4
1999 1
2001 3
2002 2
2003 1
2004 1
2005 1
2007 4
2008 1
2009 2
2010 4
2011 2
2012 1
2013 1
2014 1
2016 1
2019 1
2022 2
2024 0

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37 results

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Page 1
Epilepsy caused by CDKL5 mutations.
Castrén M, Gaily E, Tengström C, Lähdetie J, Archer H, Ala-Mello S. Castrén M, et al. Among authors: ala mello s. Eur J Paediatr Neurol. 2011 Jan;15(1):65-9. doi: 10.1016/j.ejpn.2010.04.005. Epub 2010 May 20. Eur J Paediatr Neurol. 2011. PMID: 20493745
[Update on current care guidelines: appropriate treatment of medical problems associated with Down's syndrome].
Suomalaisen Lääkäriseuran Duodecimin; Suomen Kehitysvammalääkärit--Finlands Läkare för Utvecklingsstorda RY:N Asettama Työryhmä; Kaski M, Aaltonen S, Heiskala H, Hyvärinen L, Komulainen J, Määttä T, Noponen AL, Verkasalo M, Wilska M, Ala-Mello S, Hiiri A, Sakki A. Suomalaisen Lääkäriseuran Duodecimin, et al. Among authors: ala mello s. Duodecim. 2011;127(4):364-5. Duodecim. 2011. PMID: 21442856 Review. Finnish.
Evidence for further genetic heterogeneity in nephronophthisis.
Omran H, Häffner K, Burth S, Ala-Mello S, Antignac C, Hildebrandt F. Omran H, et al. Among authors: ala mello s. Nephrol Dial Transplant. 2001 Apr;16(4):755-8. doi: 10.1093/ndt/16.4.755. Nephrol Dial Transplant. 2001. PMID: 11274269
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders.
Stoll G, Pietiläinen OPH, Linder B, Suvisaari J, Brosi C, Hennah W, Leppä V, Torniainen M, Ripatti S, Ala-Mello S, Plöttner O, Rehnström K, Tuulio-Henriksson A, Varilo T, Tallila J, Kristiansson K, Isohanni M, Kaprio J, Eriksson JG, Raitakari OT, Lehtimäki T, Jarvelin MR, Salomaa V, Hurles M, Stefansson H, Peltonen L, Sullivan PF, Paunio T, Lönnqvist J, Daly MJ, Fischer U, Freimer NB, Palotie A. Stoll G, et al. Among authors: ala mello s. Nat Neurosci. 2013 Sep;16(9):1228-1237. doi: 10.1038/nn.3484. Epub 2013 Aug 4. Nat Neurosci. 2013. PMID: 23912948 Free PMC article.
Novel PORCN mutations in focal dermal hypoplasia.
Froyen G, Govaerts K, Van Esch H, Verbeeck J, Tuomi ML, Heikkilä H, Torniainen S, Devriendt K, Fryns JP, Marynen P, Järvelä I, Ala-Mello S. Froyen G, et al. Among authors: ala mello s. Clin Genet. 2009 Dec;76(6):535-43. doi: 10.1111/j.1399-0004.2009.01248.x. Epub 2009 Oct 23. Clin Genet. 2009. PMID: 19863546
Clinical and mutational spectrum of Mowat-Wilson syndrome.
Zweier C, Thiel CT, Dufke A, Crow YJ, Meinecke P, Suri M, Ala-Mello S, Beemer F, Bernasconi S, Bianchi P, Bier A, Devriendt K, Dimitrov B, Firth H, Gallagher RC, Garavelli L, Gillessen-Kaesbach G, Hudgins L, Kääriäinen H, Karstens S, Krantz I, Mannhardt A, Medne L, Mücke J, Kibaek M, Krogh LN, Peippo M, Rittinger O, Schulz S, Schelley SL, Temple IK, Dennis NR, Van der Knaap MS, Wheeler P, Yerushalmi B, Zenker M, Seidel H, Lachmeijer A, Prescott T, Kraus C, Lowry RB, Rauch A. Zweier C, et al. Among authors: ala mello s. Eur J Med Genet. 2005 Apr-Jun;48(2):97-111. doi: 10.1016/j.ejmg.2005.01.003. Epub 2005 Feb 25. Eur J Med Genet. 2005. PMID: 16053902
Microtia in Finland: comparison of characteristics in different populations.
Suutarla S, Rautio J, Ritvanen A, Ala-Mello S, Jero J, Klockars T. Suutarla S, et al. Among authors: ala mello s. Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1211-7. doi: 10.1016/j.ijporl.2007.04.020. Epub 2007 Jun 4. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17548114
Mutation analysis of LMX1B gene in nail-patella syndrome patients.
McIntosh I, Dreyer SD, Clough MV, Dunston JA, Eyaid W, Roig CM, Montgomery T, Ala-Mello S, Kaitila I, Winterpacht A, Zabel B, Frydman M, Cole WG, Francomano CA, Lee B. McIntosh I, et al. Among authors: ala mello s. Am J Hum Genet. 1998 Dec;63(6):1651-8. doi: 10.1086/302165. Am J Hum Genet. 1998. PMID: 9837817 Free PMC article.
37 results