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Items: 41

1.

Treatment Patterns and Use of Resources in Patients With Tuberous Sclerosis Complex: Insights From the TOSCA Registry.

Marques R, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, D'Amato L, Beaure d'Augères G, de Vries PJ, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Nabbout R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Kingswood JC, Jansen AC.

Front Neurol. 2019 Oct 25;10:1144. doi: 10.3389/fneur.2019.01144. eCollection 2019.

2.

Newly Diagnosed and Growing Subependymal Giant Cell Astrocytoma in Adults With Tuberous Sclerosis Complex: Results From the International TOSCA Study.

Jansen AC, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, D'Amato L, Beaure d'Augères G, de Vries PJ, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Marques R, Nabbout R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Kingswood JC.

Front Neurol. 2019 Aug 2;10:821. doi: 10.3389/fneur.2019.00821. eCollection 2019.

3.

Clinical Characteristics of Subependymal Giant Cell Astrocytoma in Tuberous Sclerosis Complex.

Jansen AC, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, D'Amato L, d'Augères GB, de Vries PJ, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Marques R, Nabbout R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Kingswood JC.

Front Neurol. 2019 Jul 3;10:705. doi: 10.3389/fneur.2019.00705. eCollection 2019.

4.

Passive range of motion changes in young children with spastic diplegia. A study during the initial stages of independent walking.

Dimakopoulos R, Syrogiannopoulos G, Youroukos S, Dailiana Z, Spinou A.

J Pediatr Rehabil Med. 2019;12(2):151-159. doi: 10.3233/PRM-180539.

PMID:
31227665
5.

Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study.

Nabbout R, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, D Amato L, d'Augères GB, de Vries PJ, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Marques R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Jansen A, Kingswood JC; TOSCA Consortium and TOSCA Investigators.

Epilepsia Open. 2018 Dec 21;4(1):73-84. doi: 10.1002/epi4.12286. eCollection 2019 Mar.

6.

TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study.

de Vries PJ, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, D'Amato L, d'Augères GB, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Kingswood JC, Lawson JA, Macaya A, Marques R, Nabbout R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Jansen AC; TOSCA Consortium and TOSCA Investigators.

Orphanet J Rare Dis. 2018 Sep 10;13(1):157. doi: 10.1186/s13023-018-0901-8.

7.

Renal angiomyolipoma in patients with tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increase disease Awareness.

Kingswood JC, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, D' Amato L, d'Augères GB, de Vries PJ, Ferreira JC, Feucht M, Fladrowski C, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Marques R, Nabbout R, O'Callaghan F, Qin J, Sander V, Sauter M, Shah S, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Jansen AC.

Nephrol Dial Transplant. 2019 Mar 1;34(3):502-508. doi: 10.1093/ndt/gfy063.

8.

Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece.

Avgeris S, Fostira F, Vagena A, Ninios Y, Delimitsou A, Vodicka R, Vrtel R, Youroukos S, Stravopodis DJ, Vlassi M, Astrinidis A, Yannoukakos D, Voutsinas GE.

Sci Rep. 2017 Dec 1;7(1):16697. doi: 10.1038/s41598-017-16988-w.

9.

TuberOus SClerosis registry to increase disease Awareness (TOSCA) - baseline data on 2093 patients.

Kingswood JC, d'Augères GB, Belousova E, Ferreira JC, Carter T, Castellana R, Cottin V, Curatolo P, Dahlin M, de Vries PJ, Feucht M, Fladrowski C, Gislimberti G, Hertzberg C, Jozwiak S, Lawson JA, Macaya A, Nabbout R, O'Callaghan F, Benedik MP, Qin J, Marques R, Sander V, Sauter M, Takahashi Y, Touraine R, Youroukos S, Zonnenberg B, Jansen AC; TOSCA consortium and TOSCA investigators.

Orphanet J Rare Dis. 2017 Jan 5;12(1):2. doi: 10.1186/s13023-016-0553-5.

10.

Single amino acid loss in the dystrophin protein associated with a mild clinical phenotype.

Pons R, Kekou K, Gkika A, Papadimas G, Vogiatzakis N, Svingou M, Papadopooulos C, Nikas I, Dinopoulos A, Youroukos S, Kanavakis E.

Muscle Nerve. 2017 Jan;55(1):46-50. doi: 10.1002/mus.25190. Epub 2016 Oct 28.

PMID:
27178005
11.

A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings.

Polymeris AA, Tessa A, Anagnostopoulou K, Rubegni A, Galatolo D, Dinopoulos A, Gika AD, Youroukos S, Skouteli E, Santorelli FM, Pons R.

J Neurol. 2016 Aug;263(8):1604-11. doi: 10.1007/s00415-016-8179-z. Epub 2016 Jun 3.

PMID:
27260292
12.

TOSCA - first international registry to address knowledge gaps in the natural history and management of tuberous sclerosis complex.

Kingswood JC, Bruzzi P, Curatolo P, de Vries PJ, Fladrowski C, Hertzberg C, Jansen AC, Jozwiak S, Nabbout R, Sauter M, Touraine R, O'Callaghan F, Zonnenberg B, Crippa S, Comis S, d'Augères GB, Belousova E, Carter T, Cottin V, Dahlin M, Ferreira JC, Macaya A, Benedik MP, Sander V, Youroukos S, Castellana R, Ulker B, Feucht M.

Orphanet J Rare Dis. 2014 Nov 26;9:182. doi: 10.1186/s13023-014-0182-9.

13.

Juvenile myoclonic epilepsy is not associated with the DRPLA gene in a European population.

Yapijakis C, Gatzonis S, Youroukos S, Kollia V, Karachristianou S, Anagnostouli M.

In Vivo. 2014 Nov-Dec;28(6):1193-6.

PMID:
25398822
14.

Levodopa-induced dyskinesias in tyrosine hydroxylase deficiency.

Pons R, Syrengelas D, Youroukos S, Orfanou I, Dinopoulos A, Cormand B, Ormazabal A, Garzía-Cazorla A, Serrano M, Artuch R.

Mov Disord. 2013 Jul;28(8):1058-63. doi: 10.1002/mds.25382. Epub 2013 Feb 6.

PMID:
23389938
15.

Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: report of two Southern European families.

Pons R, Cuenca-León E, Miravet E, Pons M, Xaidara A, Youroukos S, Macaya A.

Eur J Paediatr Neurol. 2012 Jan;16(1):86-9. doi: 10.1016/j.ejpn.2011.09.008. Epub 2011 Oct 1.

PMID:
21962874
16.

Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation.

Pons R, Serrano M, Ormazabal A, Toma C, Garcia-Cazorla A, Area E, Ribasés M, Kanavakis E, Drakaki K, Giannakopoulos A, Orfanou I, Youroukos S, Cormand B, Artuch R.

Mov Disord. 2010 Jun 15;25(8):1086-90. doi: 10.1002/mds.23002.

PMID:
20198643
17.

A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.

Pampanos A, Volaki K, Kanavakis E, Papandreou O, Youroukos S, Thomaidis L, Karkelis S, Tzetis M, Kitsiou-Tzeli S.

Genet Test Mol Biomarkers. 2009 Oct;13(5):611-5. doi: 10.1089/gtmb.2009.0005.

PMID:
19645625
18.

Efficacy and tolerability of the new antiepileptic drugs I: treatment of new onset epilepsy: report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society.

Panayiotopoulos CP, Benbadis SR, Covanis A, Dulac O, Duncan JS, Eeg-Olofsson O, Ferrie CD, Grünewald RA, Kasteleijn-Nolst Trenité DG, Koutroumanidis M, Martinovic Z, Newton RW, Parker AP, Salas-Puig J, Sander JW, Shorvon S, Watanabe K, Whitehouse WP, Youroukos S.

Neurology. 2005 Jan 11;64(1):172-4; author reply 172-4. No abstract available.

PMID:
15645539
19.

Efficacy and tolerability of the new antiepileptic drugs: commentary on the recently published practice parameters.

Panayiotopoulos CP, Benbadis SR, Covanis A, Dulac O, Duncan JS, Eeg-Olofsson O, Ferrie CD, Grünewald RA, Kasteleijn-Nolst Trenite DG, Koutroumanidis M, Martinovic Z, Newton RW, Parker AP, Salas-Puig J, Sander JW, Shorvon S, Watanabe K, Whitehouse WP, Youroukos S.

Epilepsia. 2004 Dec;45(12):1646-9; author reply 1649-51. No abstract available.

20.

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.

Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF, Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos S.

Ann Neurol. 2004 Jun;55(6):884-7.

PMID:
15174025
21.

Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait.

Kanavakis E, Xaidara A, Papathanasiou-Klontza D, Papadimitriou A, Velentza S, Youroukos S.

Dev Med Child Neurol. 2003 Dec;45(12):833-6. Erratum in: Dev Med Child Neurol. 2004 Apr;46(4):288.

22.

Acute psychosis associated with levetiracetam.

Youroukos S, Lazopoulou D, Michelakou D, Karagianni J.

Epileptic Disord. 2003 Jun;5(2):117-9.

23.

Campylobacter jejuni O:19 serotype-associated Guillain-Barré syndrome in a child: the first case reported from Greece.

Chatzipanagiotou S, Kilidireas K, Trimis G, Nicolaou C, Anagnostouli M, Athanassaki C, Giannoulia A, Legakis N, Youroukos S.

Clin Microbiol Infect. 2003 Jan;9(1):69-72.

24.

Outbreak of enteroviral infection in a pediatric hematology-oncology unit.

Moschovi MA, Theodoridou M, Papaevangelou V, Youroukos S, Nitsa A, Matsiota P, Tzortzatou-Stathopoulou F.

Clin Infect Dis. 2002 May 1;34(9):1269-72. Epub 2002 Apr 2.

PMID:
11941555
25.

Encephalitis and myocarditis in a child with acute lymphoblastic leukemia: role of coxsackievirus B5?

Moschovi M, Sterpi P, Youroukos S, Tzortzatou-Stathopoulou F.

Pediatr Hematol Oncol. 2002 Apr-May;19(3):205-10. Erratum in: Pediatr Hematol Oncol. 2002 Sep;19(6):449.. Moscjovi Maria A [corrected to Moschovi Mary].

PMID:
11936734
26.

Posterior cerebral artery occlusion associated with Mycoplasma pneumoniae infection.

Antachopoulos C, Liakopoulou T, Palamidou F, Papathanassiou D, Youroukos S.

J Child Neurol. 2002 Jan;17(1):55-7.

PMID:
11913573
27.

Late recurrence of herpes simplex virus meningoencephalitis in two infants.

Mandyla H, Anagnostakis D, Koutsovitis P, Siahanidou T, Youroukos S.

Eur J Pediatr. 2001 Dec;160(12):732-5.

PMID:
11795682
28.

Continuous neostigmine infusion in post-thymectomy juvenile myasthenic crisis.

Briassoulis G, Hatzis T, Liakopoulou T, Youroukos S.

J Child Neurol. 2000 Nov;15(11):747-9.

PMID:
11108508
29.

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.

Eunson LH, Rea R, Zuberi SM, Youroukos S, Panayiotopoulos CP, Liguori R, Avoni P, McWilliam RC, Stephenson JB, Hanna MG, Kullmann DM, Spauschus A.

Ann Neurol. 2000 Oct;48(4):647-56.

PMID:
11026449
30.

Idiopathic intracranial hypertension in children.

Youroukos S, Psychou F, Fryssiras S, Paikos P, Nicolaidou P.

J Child Neurol. 2000 Jul;15(7):453-7.

PMID:
10921516
31.

Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients.

Kekou K, Mavrou A, Florentin L, Youroukos S, Zafiriou DI, Skouteli HN, Metaxotou C.

Eur J Hum Genet. 1999 Feb-Mar;7(2):179-87.

32.

Diet during pregnancy and the risk of cerebral palsy.

Petridou E, Koussouri M, Toupadaki N, Youroukos S, Papavassiliou A, Pantelakis S, Olsen J, Trichopoulos D.

Br J Nutr. 1998 May;79(5):407-12.

PMID:
9682658
33.

Epilepsy in patients with cerebral palsy.

Hadjipanayis A, Hadjichristodoulou C, Youroukos S.

Dev Med Child Neurol. 1997 Oct;39(10):659-63.

34.

Risk factors for cerebral palsy: a case-control study in Greece.

Petridou E, Koussouri M, Toupadaki N, Papavassiliou A, Youroukos S, Katsarou E, Trichopoulos D.

Scand J Soc Med. 1996 Mar;24(1):14-26.

PMID:
8740872
35.

Birth weight and handedness in boys and girls.

Petridou E, Flytzani V, Youroukos S, Lee IM, Yen YY, Tong D, Trichopoulos D.

Hum Biol. 1994 Dec;66(6):1093-101.

PMID:
7835873
36.

Relapse of herpes simplex encephalitis after acyclovir therapy.

Nicolaidou P, Iacovidou N, Youroukos S, Liacopoulou-Tsitsipi T, Kattamis C.

Eur J Pediatr. 1993 Sep;152(9):737-8.

PMID:
8223804
37.

Genetics and fetal hydantoin syndrome.

Karpathios T, Zervoudakis A, Venieris F, Parchas S, Youroukos S.

Acta Paediatr Scand. 1989 Jan;78(1):125-6. No abstract available.

PMID:
2493186
38.

Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient.

Mavrou A, Syrrou M, Tsenghi C, Agelakis M, Youroukos S, Metaxotou C.

Am J Med Genet. 1988 Dec;31(4):735-9.

PMID:
3239562
39.

C.A.T. scan in severe facial cleft surgery. Case report.

Christophorou M, Youroukos S, Yiacoumettis A.

J Maxillofac Surg. 1981 Aug;9(3):185-7. No abstract available.

PMID:
6944420
40.

Porencephalic cysts after amniocentesis.

Youroukos S, Papadelis F, Matsaniotis N.

Arch Dis Child. 1980 Oct;55(10):814-5.

41.

Increased blood lead levels in mentally retarded children in Greece.

Youroukos S, Lyberatos C, Philippidou A, Gardikas C, Tsomi A.

Arch Environ Health. 1978 Nov-Dec;33(6):297-300.

PMID:
736612

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