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Publikationen

Suchbegriffe: AGE OF ONSET - , . Treffer: 101

2019

Skrabl-Baumgartner, A; Singer, P; Greimel, T; Gorkiewicz, G; Hermann, J Chronic non-bacterial osteomyelitis: a comparative study between children and adults.
Pediatr Rheumatol Online J. 2019; 17(1):49-49 Doi: 10.1186/s12969-019-0353-2 [OPEN ACCESS]
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2018

de Rooy, RLP; Halbertsma, FJ; Struijs, EA; van Spronsen, FJ; Lunsing, RJ; Schippers, HM; van Hasselt, PM; Plecko, B; Wohlrab, G; Whalen, S; Benoist, JF; Valence, S; Mills, PB; Bok, LA Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?
Eur J Paediatr Neurol. 2018; 22(4): 662-666. Doi: 10.1016/j.ejpn.2018.03.009
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Hamilton, EMC; van der Lei, HDW; Vermeulen, G; Gerver, JAM; Lourenço, CM; Naidu, S; Mierzewska, H; Gemke, RJBJ; de Vet, HCW; Uitdehaag, BMJ; Lissenberg-Witte, BI; VWM Research Group; van der Knaap, MS Natural History of Vanishing White Matter.
Ann Neurol. 2018; 84(2):274-288 Doi: 10.1002/ana.25287 [OPEN ACCESS]
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Löscher, WN; Huemer, M; Stulnig, TM; Simschitz, P; Iglseder, S; Eggers, C; Moser, H; Möslinger, D; Freilinger, M; Lagler, F; Grinzinger, S; Reichhardt, M; Bittner, RE; Schmidt, WM; Lex, U; Brunner-Krainz, M; Quasthoff, S; Wanschitz, JV Pompe disease in Austria: clinical, genetic and epidemiological aspects.
J Neurol. 2018; 265(1):159-164 Doi: 10.1007/s00415-017-8686-6 [OPEN ACCESS]
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Löscher, WN; Oberreiter, EM; Erdler, M; Quasthoff, S; Culea, V; Berek, K; Embacher, N; Grinzinger, S; Hess, I; Höger, FS; Horlings, CGC; Huemer, M; Jecel, J; Kleindienst, W; Laich, E; Müller, P; Oel, D; Örtl, W; Lenzenweger, E; Rath, J; Stadler, K; Stieglbauer, K; Thaler-Wolf, C; Wanschitz, J; Zimprich, F; Cetin, H; Topakian, R Multifocal motor neuropathy in Austria: a nationwide survey of clinical features and response to treatment.
J NEUROL. 2018; 265(12): 2834-2840. Doi: 10.1007/s00415-018-9071-9 [OPEN ACCESS]
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Mahmud, FH; Elbarbary, NS; Fröhlich-Reiterer, E; Holl, RW; Kordonouri, O; Knip, M; Simmons, K; Craig, ME ISPAD Clinical Practice Consensus Guidelines 2018: Other complications and associated conditions in children and adolescents with type 1 diabetes.
Pediatr Diabetes. 2018; 19 Suppl 27(1):275-286 Doi: 10.1111/pedi.12740 [OPEN ACCESS]
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2017

Skrabl-Baumgartner, A; Christine Hauer, A; Erwa, W; Jahnel, J HLA genotyping as first-line screening tool for coeliac disease in children with juvenile idiopathic arthritis.
Arch Dis Child. 2017; 102(7):607-611 Doi: 10.1136/archdischild-2016-311544
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Zhang, D; Kaufmann, WE; Sigafoos, J; Bartl-Pokorny, KD; Krieber, M; Marschik, PB; Einspieler, C Parents' initial concerns about the development of their children later diagnosed with fragile X syndrome.
J Intellect Dev Disabil. 2017; 42(2):114-122 Doi: 10.3109/13668250.2016.1228858 [OPEN ACCESS]
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2016

Auer-Grumbach, M; Toegel, S; Schabhüttl, M; Weinmann, D; Chiari, C; Bennett, DLH; Beetz, C; Klein, D; Andersen, PM; Böhme, I; Fink-Puches, R; Gonzalez, M; Harms, MB; Motley, W; Reilly, MM; Renner, W; Rudnik-Schöneborn, S; Schlotter-Weigel, B; Themistocleous, AC; Weishaupt, JH; Ludolph, AC; Wieland, T; Tao, F; Abreu, L; Windhager, R; Zitzelsberger, M; Strom, TM; Walther, T; Scherer, SS; Züchner, S; Martini, R; Senderek, J Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
Am J Hum Genet. 2016; 99(3):607-623 Doi: 10.1016/j.ajhg.2016.07.008 [OPEN ACCESS]
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Kong, X; Strauss, RW; Michaelides, M; Cideciyan, AV; Sahel, JA; Muñoz, B; West, S; Scholl, HP; ProgStar Study Group Visual Acuity Loss and Associated Risk Factors in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2).
Ophthalmology. 2016; 123(9):1887-1897 Doi: 10.1016/j.ophtha.2016.05.027
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San Giorgi, MR; van den Heuvel, ER; Tjon Pian Gi, RE; Brunings, JW; Chirila, M; Friedrich, G; Golusinski, W; Graupp, M; Horcasitas Pous, RA; Ilmarinen, T; Jackowska, J; Koelmel, JC; Ferran Vilà, F; Weichbold, V; Wierzbicka, M; Dikkers, FG Age of onset of recurrent respiratory papillomatosis: a distribution analysis.
Clin Otolaryngol. 2016; 41(5):448-453 Doi: 10.1111/coa.12565
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2015

Do, R; Stitziel, NO; Won, HH; Jørgensen, AB; Duga, S; Angelica Merlini, P; Kiezun, A; Farrall, M; Goel, A; Zuk, O; Guella, I; Asselta, R; Lange, LA; Peloso, GM; Auer, PL; NHLBI Exome Sequencing Project; Girelli, D; Martinelli, N; Farlow, DN; DePristo, MA; Roberts, R; Stewart, AF; Saleheen, D; Danesh, J; Epstein, SE; Sivapalaratnam, S; Hovingh, GK; Kastelein, JJ; Samani, NJ; Schunkert, H; Erdmann, J; Shah, SH; Kraus, WE; Davies, R; Nikpay, M; Johansen, CT; Wang, J; Hegele, RA; Hechter, E; Marz, W; Kleber, ME; Huang, J; Johnson, AD; Li, M; Burke, GL; Gross, M; Liu, Y; Assimes, TL; Heiss, G; Lange, EM; Folsom, AR; Taylor, HA; Olivieri, O; Hamsten, A; Clarke, R; Reilly, DF; Yin, W; Rivas, MA; Donnelly, P; Rossouw, JE; Psaty, BM; Herrington, DM; Wilson, JG; Rich, SS; Bamshad, MJ; Tracy, RP; Cupples, LA; Rader, DJ; Reilly, MP; Spertus, JA; Cresci, S; Hartiala, J; Tang, WH; Hazen, SL; Allayee, H; Reiner, AP; Carlson, CS; Kooperberg, C; Jackson, RD; Boerwinkle, E; Lander, ES; Schwartz, SM; Siscovick, DS; McPherson, R; Tybjaerg-Hansen, A; Abecasis, GR; Watkins, H; Nickerson, DA; Ardissino, D; Sunyaev, SR; O'Donnell, CJ; Altshuler, D; Gabriel, S; Kathiresan, S Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
NATURE. 2015; 518(7537): 102-106. Doi: 10.1038/nature13917 [OPEN ACCESS]
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Huemer, M; Bürer, C; Ješina, P; Kožich, V; Landolt, MA; Suormala, T; Fowler, B; Augoustides-Savvopoulou, P; Blair, E; Brennerova, K; Broomfield, A; De Meirleir, L; Gökcay, G; Hennermann, J; Jardine, P; Koch, J; Lorenzl, S; Lotz-Havla, AS; Noss, J; Parini, R; Peters, H; Plecko, B; Ramos, FJ; Schlune, A; Tsiakas, K; Zerjav Tansek, M; Baumgartner, MR Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data.
J Inherit Metab Dis. 2015; 38(5):957-967 Doi: 10.1007/s10545-014-9803-7
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Kapfhammer, HP; Huppert, D; Grill, E; Fitz, W; Brandt, T Visual height intolerance and acrophobia: clinical characteristics and comorbidity patterns.
EUR PSYCHIAT. 2015; 265(5): 375-385. Doi: 10.1007/s00406-014-0548-y [Oral Communication]
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Pont-Sunyer, C; Hotter, A; Gaig, C; Seppi, K; Compta, Y; Katzenschlager, R; Mas, N; Hofeneder, D; Brücke, T; Bayés, A; Wenzel, K; Infante, J; Zach, H; Pirker, W; Posada, IJ; Álvarez, R; Ispierto, L; De Fàbregues, O; Callén, A; Palasí, A; Aguilar, M; Martí, MJ; Valldeoriola, F; Salamero, M; Poewe, W; Tolosa, E The onset of nonmotor symptoms in Parkinson's disease (the ONSET PD study).
Mov Disord. 2015; 30(2):229-237 Doi: 10.1002/mds.26077
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Rohrer, TR; Wolf, J; Liptay, S; Zimmer, KP; Fröhlich-Reiterer, E; Scheuing, N; Marg, W; Stern, M; Kapellen, TM; Hauffa, BP; Wölfle, J; Holl, RW; DPV Initiative and the German BMBF Competence Network Diabetes Mellitus Microvascular Complications in Childhood-Onset Type 1 Diabetes and Celiac Disease: A Multicenter Longitudinal Analysis of 56,514 Patients From the German-Austrian DPV Database.
Diabetes Care. 2015; 38(5):801-807 Doi: 10.2337/dc14-0683 [OPEN ACCESS]
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Sadowski, CE; Lovric, S; Ashraf, S; Pabst, WL; Gee, HY; Kohl, S; Engelmann, S; Vega-Warner, V; Fang, H; Halbritter, J; Somers, MJ; Tan, W; Shril, S; Fessi, I; Lifton, RP; Bockenhauer, D; El-Desoky, S; Kari, JA; Zenker, M; Kemper, MJ; Mueller, D; Fathy, HM; Soliman, NA; SRNS Study Group; Hildebrandt, F A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
J Am Soc Nephrol. 2015; 26(6): 1279-1289. Doi: 10.1681/ASN.2014050489 [OPEN ACCESS]
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2014

Bechtold, S; Blaschek, A; Raile, K; Dost, A; Freiberg, C; Askenas, M; Fröhlich-Reiterer, E; Molz, E; Holl, RW Higher relative risk for multiple sclerosis in a pediatric and adolescent diabetic population: analysis from DPV database.
Diabetes Care. 2014; 37(1):96-101 Doi: 10.2337/dc13-1414 [OPEN ACCESS]
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Broganelli, P; Titli, S; Lallas, A; Alaibac M Annetta, A; Battarra, V; Brunetti, B; Castagno, I; Cavicchini, S; Ferrari, A; Ghigliotti, G; Landi, C; Manganoni, A; Moscarella, E; Pellacani, G; Pizzichetta, MA; Rosina, P; Rubegni, P; Satta, R; Scalvenzi, M; Stanganelli, I; Stinco, G; Zalaudek, I; Zampieri, P; Argenziano, G; Dermoscopy Study Group of the Italian Society of Dermatology Spitz/Reed nevi: proposal of management recommendations by the Dermoscopy Study Group of the Italian Society of Dermatology (SIDeMaST).
G Ital Dermatol Venereol. 2014; 149(5):601-606
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Ganos, C; Aguirregomozcorta, M; Batla, A; Stamelou, M; Schwingenschuh, P; Münchau, A; Edwards, MJ; Bhatia, KP Psychogenic paroxysmal movement disorders--clinical features and diagnostic clues.
Parkinsonism Relat Disord. 2014; 20(1):41-46 Doi: 10.1016/j.parkreldis.2013.09.012 [OPEN ACCESS]
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Khalil, M; Riedlbauer, B; Langkammer, C; Enzinger, C; Ropele, S; Stojakovic, T; Scharnagl, H; Culea, V; Petzold, A; Teunissen, C; Archelos, JJ; Fuchs, S; Fazekas, F Cerebrospinal fluid transferrin levels are reduced in patients with early multiple sclerosis.
Mult Scler. 2014; 20(12):1569-1577 Doi: 10.1177/1352458514530020
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Lackner, N; Birner, A; Bengesser, SA; Reininghaus, B; Kapfhammer, HP; Reininghaus, E [Pediatric bipolar disorder - case report of a bipolar patient with disease onset in childhood and adolescence: implications for diagnosis and therapy].
Fortschr Neurol Psychiatr. 2014; 82(11):646-654 Doi: 10.1055/s-0034-1385271 (- Case Report)
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Miller, DH; Fazekas, F; Montalban, X; Reingold, SC; Trojano, M Pregnancy, sex and hormonal factors in multiple sclerosis.
MULT SCLER J. 2014; 20(5): 527-536. Doi: 10.1177/1352458513519840 [OPEN ACCESS]
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Rüegger, CM; Lindner, M; Ballhausen, D; Baumgartner, MR; Beblo, S; Das, A; Gautschi, M; Glahn, EM; Grünert, SC; Hennermann, J; Hochuli, M; Huemer, M; Karall, D; Kölker, S; Lachmann, RH; Lotz-Havla, A; Möslinger, D; Nuoffer, JM; Plecko, B; Rutsch, F; Santer, R; Spiekerkoetter, U; Staufner, C; Stricker, T; Wijburg, FA; Williams, M; Burgard, P; Häberle, J Cross-sectional observational study of 208 patients with non-classical urea cycle disorders.
J Inherit Metab Dis. 2014; 37(1):21-30 Doi: 10.1007/s10545-013-9624-0 [OPEN ACCESS]
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2013

Biazar, C; Sigges, J; Patsinakidis, N; Ruland, V; Amler, S; Bonsmann, G; Kuhn, A; EUSCLE co-authors Cutaneous lupus erythematosus: first multicenter database analysis of 1002 patients from the European Society of Cutaneous Lupus Erythematosus (EUSCLE).
Autoimmun Rev. 2013; 12(3): 444-454. Doi: 10.1016/j.autrev.2012.08.019
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Brunasso, AM; Puntoni, M; Aberer, W; Delfino, C; Fancelli, L; Massone, C Clinical and epidemiological comparison of patients affected by palmoplantar plaque psoriasis and palmoplantar pustulosis: a case series study.
Br J Dermatol. 2013; 168(6):1243-1251 Doi: 10.1111/bjd.12223
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Dejaco, C; Duftner, C; Wipfler-Freißmuth, E; Weiss, H; Schneider, T; Schirmer, M Elderly versus young onset rheumatoid arthritis: Higher levels of ultrasound-detected inflammation despite comparable clinical disease activity.
Arthritis Care Res (Hoboken). 2013; 65(2):304-308 Doi: 10.1002/acr.21823 [OPEN ACCESS]
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European Alzheimer's Disease Initiative (EADI); Genetic and Environmental Risk in Alzheimer's Disease; Alzheimer's Disease Genetic Consortium; Cohorts for Heart and Aging Research in Genomic Epidemiology Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
Nat Genet. 2013; 45(12):1452-1458 Doi: 10.1038/ng.2802 [OPEN ACCESS]
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Fritsch, M; Schober, E; Rami-Merhar, B; Hofer, S; Fröhlich-Reiterer, E; Waldhoer, T; Austrian Diabetes Incidence Study Group Diabetic ketoacidosis at diagnosis in Austrian children: a population-based analysis, 1989-2011.
J Pediatr. 2013; 163(5):1484-1488 Doi: 10.1016/j.jpeds.2013.06.033
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Giorgio, A; Battaglini, M; Rocca, MA; De Leucio, A; Absinta, M; van Schijndel, R; Rovira, A; Tintoré, M; Chard, D; Ciccarelli, O; Enzinger, C; Gasperini, C; Frederiksen, J; Filippi, M; Barkhof, F; De Stefano, N; on behalf of the MAGNIMS Study Group Location of brain lesions predicts conversion of clinically isolated syndromes to multiple sclerosis.
Neurology. 2013; 80(3):234-241 Doi: 10.1212/WNL.0b013e31827debeb
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Kangozhinova, K; Abentayeva, B; Repa, A; Baltabayeva, A; Erwa, W; Stauffer, F Culture proven newborn sepsis with a special emphasis on late onset sepsis caused by Enterobacteriaceae in a level III neonatal care unit in Astana, Kazakhstan.
Wien Klin Wochenschr. 2013; 125(19-20):611-615 Doi: 10.1007/s00508-013-0416-1
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Metzger, S; Walter, C; Riess, O; Roos, RA; Nielsen, JE; Craufurd, D; REGISTRY Investigators of the European Huntington’s Disease Network; Nguyen, HP The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients.
PLoS One. 2013; 8(7):e68951-e68951 Doi: 10.1371/journal.pone.0068951 [OPEN ACCESS]
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Papay, P; Miehsler, W; Tilg, H; Petritsch, W; Reinisch, W; Mayer, A; Haas, T; Kaser, A; Feichtenschlager, T; Fuchssteiner, H; Knoflach, P; Vogelsang, H; Platzer, R; Tillinger, W; Jaritz, B; Schmid, A; Blaha, B; Dejaco, C; Sobala, A; Weltermann, A; Eichinger, S; Novacek, G Clinical presentation of venous thromboembolism in inflammatory bowel disease.
J Crohns Colitis. 2013; 7(9):723-729 Doi: 10.1016/j.crohns.2012.10.008 [OPEN ACCESS]
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Pichler, A; Enzinger, C; Fuchs, S; Plecko-Startinig, B; Gruber-Sedlmayr, U; Linortner, P; Langkammer, C; Khalil, M; Ebner, F; Ropele, S; Fazekas, F Differences and similarities in the evolution of morphologic brain abnormalities between paediatric and adult-onset multiple sclerosis.
Mult Scler. 2013; 19(2):167-172 Doi: 10.1177/1352458512448107
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2012

de Vries, E; European Society for Immunodeficiencies (ESID) members Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update.
Clin Exp Immunol. 2012; 167(1): 108-119. Doi: 10.1111/j.1365-2249.2011.04461.x [OPEN ACCESS]
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Gerber, NU; von Hoff, K; von Bueren, AO; Treulieb, W; Deinlein, F; Benesch, M; Zwiener, I; Soerensen, N; Warmuth-Metz, M; Pietsch, T; Mittler, U; Kuehl, J; Kortmann, RD; Grotzer, MA; Rutkowski, S A long duration of the prediagnostic symptomatic interval is not associated with an unfavourable prognosis in childhood medulloblastoma.
Eur J Cancer. 2012; 48(13):2028-2036 Doi: 10.1016/j.ejca.2011.11.012 [OPEN ACCESS]
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Holl, AK; Wilkinson, L; Tabrizi, SJ; Painold, A; Jahanshahi, M Probabilistic classification learning with corrective feedback is selectively impaired in early Huntington's disease-Evidence for the role of the striatum in learning with feedback.
Neuropsychologia. 2012; 50(9):2176-2186 Doi: 10.1016/j.neuropsychologia.2012.05.021
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Schmied, MC; Zehetmayer, S; Reindl, M; Ehling, R; Bajer-Kornek, B; Leutmezer, F; Zebenholzer, K; Hotzy, C; Lichtner, P; Meitinger, T; Wichmann, HE; Illig, T; Gieger, C; Huber, K; Khalil, M; Fuchs, S; Schmidt, H; Auff, E; Kristoferitsch, W; Fazekas, F; Berger, T; Vass, K; Zimprich, A Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.
Neurogenetics. 2012; 13(2):181-187 Doi: 10.1007/s10048-012-0316-y
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Steigleder-Schweiger, C; Rami-Merhar, B; Waldhör, T; Fröhlich-Reiterer, E; Schwarz, I; Fritsch, M; Borkenstein, M; Schober, E Prevalence of cardiovascular risk factors in children and adolescents with type 1 diabetes in Austria.
Eur J Pediatr. 2012; 171(8):1193-1202 Doi: 10.1007/s00431-012-1704-x
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2011

Baets, J; Deconinck, T; De Vriendt, E; Zimoń, M; Yperzeele, L; Van Hoorenbeeck, K; Peeters, K; Spiegel, R; Parman, Y; Ceulemans, B; Van Bogaert, P; Pou-Serradell, A; Bernert, G; Dinopoulos, A; Auer-Grumbach, M; Sallinen, SL; Fabrizi, GM; Pauly, F; Van den Bergh, P; Bilir, B; Battaloglu, E; Madrid, RE; Kabzińska, D; Kochanski, A; Topaloglu, H; Miller, G; Jordanova, A; Timmerman, V; De Jonghe, P Genetic spectrum of hereditary neuropathies with onset in the first year of life.
Brain. 2011; 134(Pt 9):2664-2676 Doi: 10.1093/brain/awr184 [OPEN ACCESS]
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Cvitanovic-Sojat, L; Gjergja Juraski, R; Sabourdy, F; Fensom, AH; Fumic, K; Paschke, E; Levade, T Farber lipogranulomatosis type 1--late presentation and early death in a Croatian boy with a novel homozygous ASAH1 mutation.
Eur J Paediatr Neurol. 2011; 15(2):171-173 Doi: 10.1016/j.ejpn.2010.06.002 (- Case Report)
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Damasio, J; Edwards, MJ; Alonso-Canovas, A; Schwingenschuh, P; Kagi, G; Bhatia, KP The clinical syndrome of primary tic disorder associated with dystonia: a large clinical series and a review of the literature.
Mov Disord. 2011; 26(4):679-684 Doi: 10.1002/mds.23484
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Fritsch, M; Rosenbauer, J; Schober, E; Neu, A; Placzek, K; Holl, RW; German Competence Network Diabetes Mellitus and the DPV Initiative Predictors of diabetic ketoacidosis in children and adolescents with type 1 diabetes. Experience from a large multicentre database.
Pediatr Diabetes. 2011; 12(4 Pt 1): 307-312. Doi: 10.1111/j.1399-5448.2010.00728.x
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Katschnig, P; Massano, J; Edwards, MJ; Schwingenschuh, P; Cordivari, C; Bhatia, KP Late-onset asymmetric myoclonus: An emerging syndrome.
Mov Disord. 2011; 26(9):1744-1747 Doi: 10.1002/mds.23676
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Pfarr, N; Szamalek-Hoegel, J; Fischer, C; Hinderhofer, K; Nagel, C; Ehlken, N; Tiede, H; Olschewski, H; Reichenberger, F; Ghofrani, AH; Seeger, W; Grünig, E Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations.
Respir Res. 2011; 12(12):99-99 Doi: 10.1186/1465-9921-12-99 [OPEN ACCESS]
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Saxena, AK; Castellani, C; Zaupa, P; Höllwarth, ME Pre-pubertal presentation of peritoneal inclusion cyst associated with congenital lower extremity venous valve agenesis.
JSLS. 2011; 15(2): 264-267. Doi: 10.4293/108680811X13071180406835 (- Case Report) [OPEN ACCESS]
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Silbernagel, G; Renner, W; Grammer, TB; Hugl, SR; Bertram, J; Kleber, ME; Hoffmann, MM; Winkelmann, BR; Marz, W; Boehm, BO Association of TCF7L2 SNPs with age at onset of type 2 diabetes and proinsulin/insulin ratio but not with glucagon-like peptide 1
DIABETES-METAB RES. 2011; 27(5): 499-505. Doi: 10.1002/dmrr.1194 [OPEN ACCESS]
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Williams, T; Machann, W; Kühler, L; Hamm, H; Müller-Höcker, J; Zimmer, M; Ertl, G; Ritter, O; Beer, M; Schönberger, J Novel desmoplakin mutation: juvenile biventricular cardiomyopathy with left ventricular non-compaction and acantholytic palmoplantar keratoderma.
Clin Res Cardiol. 2011; 100(12):1087-1093 Doi: 10.1007/s00392-011-0345-9 (- Case Report) [OPEN ACCESS]
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2010

Fioredda, F; Moser, A; Bertoluzzo, L; Lackner, H; Giacchino, R; Laspina, M; Lazier, L; Riva, C; Giacchino, M; Fraschini, D; Frey, E; Sementa, A; Pistorio, A; Haupt, R; On behalf of I-BFM ELTEC (Early and Late Toxicity Educational Committee) Natural course of HCV infection in childhood cancer survivors.
Support Care Cancer. 2010; 18(11):1413-1420 Doi: 10.1007/s00520-009-0763-7
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Houlden, H; Schneider, SA; Paudel, R; Melchers, A; Schwingenschuh, P; Edwards, M; Hardy, J; Bhatia, KP THAP1 mutations (DYT6) are an additional cause of early-onset dystonia.
Neurology. 2010; 74(10): 846-850. Doi: 10.1212/WNL.0b013e3181d5276d [OPEN ACCESS]
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