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2. An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease. Biancheri R; Verbeek E; Rossi A; Gaggero R; Roccatagliata L; Gatti R; van Diggelen O; Verheijen FW; Mancini GM Clin Genet; 2002 Jun; 61(6):443-7. PubMed ID: 12121352 [TBL] [Abstract][Full Text] [Related]
3. A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla Disease. Barmherzig R; Bullivant G; Cordeiro D; Sinasac DS; Blaser S; Mercimek-Mahmutoglu S Pediatr Neurol; 2017 Sep; 74():87-91.e2. PubMed ID: 28662915 [TBL] [Abstract][Full Text] [Related]
4. Salla disease in Turkish children: severe and conventional type. Coker M; Kalkan-Uçar S; Kitiş O; Uçar H; Gökşen-Simşek D; Darcan S; Gökben S Turk J Pediatr; 2009; 51(6):605-9. PubMed ID: 20196397 [TBL] [Abstract][Full Text] [Related]
5. Novel form of intermediate salla disease: clinical and neuroimaging features. Morse RP; Kleta R; Alroy J; Gahl WA J Child Neurol; 2005 Oct; 20(10):814-6. PubMed ID: 16417876 [TBL] [Abstract][Full Text] [Related]
7. Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease. Tarailo-Graovac M; Drögemöller BI; Wasserman WW; Ross CJ; van den Ouweland AM; Darin N; Kollberg G; van Karnebeek CD; Blomqvist M Orphanet J Rare Dis; 2017 Feb; 12(1):28. PubMed ID: 28187749 [TBL] [Abstract][Full Text] [Related]
8. Clinical, biochemical, and molecular diagnosis of a free sialic acid storage disease patient of moderate severity. Kleta R; Morse RP; Orvisky E; Krasnewich D; Alroy J; Ucci AA; Bernardini I; Wenger DA; Gahl WA Mol Genet Metab; 2004 Jun; 82(2):137-43. PubMed ID: 15172001 [TBL] [Abstract][Full Text] [Related]
9. Infantile sialic acid storage disease: serial ultrasound and magnetic resonance imaging features. Parazzini C; Arena S; Marchetti L; Menni F; Filocamo M; Verheijen FW; Mancini GM; Triulzi F; Parini R AJNR Am J Neuroradiol; 2003 Mar; 24(3):398-400. PubMed ID: 12637289 [No Abstract] [Full Text] [Related]
10. A case of Salla disease with involvement of the cerebellar white matter. Linnankivi T; Lönnqvist T; Autti T Neuroradiology; 2003 Feb; 45(2):107-9. PubMed ID: 12592494 [TBL] [Abstract][Full Text] [Related]
11. A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindred. Landau D; Cohen D; Shalev H; Pinsk V; Yerushalmi B; Zeigler M; Birk OS Mol Genet Metab; 2004 Jun; 82(2):167-72. PubMed ID: 15172005 [TBL] [Abstract][Full Text] [Related]
14. [Salla disease in Danish children. The first two cases of Salla disease in Danish children]. Christensen PS; Kaad PH; Ostergaard JR Ugeskr Laeger; 2005 May; 167(21):2292-3. PubMed ID: 15962859 [No Abstract] [Full Text] [Related]
15. Increased brain glucose utilization in Salla disease (free sialic acid storage disorder). Suhonen-Polvi H; Varho T; Metsähonkala L; Haataja L; Ruotsalainen U; Haaparanta M; Bergman J; Solin O; Aärimaa T; Holopainen I; Vainionpää L; Manner T; Jääskeläinen S; Renlund M; Sillanpää M; Aula P J Nucl Med; 1999 Jan; 40(1):12-8. PubMed ID: 9935050 [TBL] [Abstract][Full Text] [Related]
16. A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases. Verheijen FW; Verbeek E; Aula N; Beerens CE; Havelaar AC; Joosse M; Peltonen L; Aula P; Galjaard H; van der Spek PJ; Mancini GM Nat Genet; 1999 Dec; 23(4):462-5. PubMed ID: 10581036 [TBL] [Abstract][Full Text] [Related]