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Items: 1 to 50 of 82

1.

Neurodevelopmental problems of unaccompanied refugee and migrant children: a new challenge for pediatric neurologists.

Fazzi E, Korff C, Bernabe Gelot A, Leroy P, Rivier F, San Antonio-Arce V, Veggiotti P.

Dev Med Child Neurol. 2019 Jun 10. doi: 10.1111/dmcn.14275. [Epub ahead of print] No abstract available.

PMID:
31183863
2.

The spectrum of intermediate SCN8A-related epilepsy.

Johannesen KM, Gardella E, Encinas AC, Lehesjoki AE, Linnankivi T, Petersen MB, Lund ICB, Blichfeldt S, Miranda MJ, Pal DK, Lascelles K, Procopis P, Orsini A, Bonuccelli A, Giacomini T, Helbig I, Fenger CD, Sisodiya SM, Hernandez-Hernandez L, Krithika S, Rumple M, Masnada S, Valente M, Cereda C, Giordano L, Accorsi P, Bürki SE, Mancardi M, Korff C, Guerrini R, von Spiczak S, Hoffman-Zacharska D, Mazurczak T, Coppola A, Buono S, Vecchi M, Hammer MF, Varesio C, Veggiotti P, Lal D, Brünger T, Zara F, Striano P, Rubboli G, Møller RS.

Epilepsia. 2019 May;60(5):830-844. doi: 10.1111/epi.14705. Epub 2019 Apr 10.

PMID:
30968951
3.

Clinical and genetic spectrum of SCN2A-associated episodic ataxia.

Schwarz N, Bast T, Gaily E, Golla G, Gorman KM, Griffiths LR, Hahn A, Hukin J, King M, Korff C, Miranda MJ, Møller RS, Neubauer B, Smith RA, Smol T, Striano P, Stroud B, Vaccarezza M, Kluger G, Lerche H, Fazeli W.

Eur J Paediatr Neurol. 2019 May;23(3):438-447. doi: 10.1016/j.ejpn.2019.03.001. Epub 2019 Mar 7.

PMID:
30928199
4.

Comment on: Ketogenic diet treatment in recurrent diffuse intrinsic pontine glioma in children: A safety and feasibility study.

Perez A, Merlini L, El-Ayadi M, Korff C, Ansari M, von Bueren AO.

Pediatr Blood Cancer. 2019 Jul;66(7):e27664. doi: 10.1002/pbc.27664. Epub 2019 Feb 15. No abstract available.

PMID:
30767367
5.

Why the TimeToStop trial failed to recruit: a survey on antiepileptic drug withdrawal after paediatric epilepsy surgery.

Lamberink HJ, Geleijns K, Otte WM, Arzimanoglou A, Helen Cross J, Korff CM, Ramantani G, Braun KPJ.

Epileptic Disord. 2018 Oct 1;20(5):374-385. doi: 10.1684/epd.2018.1003.

PMID:
30378554
6.

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

Mulhern MS, Stumpel C, Stong N, Brunner HG, Bier L, Lippa N, Riviello J, Rouhl RPW, Kempers M, Pfundt R, Stegmann APA, Kukolich MK, Telegrafi A, Lehman A; CAUSES study, Lopez-Rangel E, Houcinat N, Barth M, den Hollander N, Hoffer MJV, Weckhuysen S; EuroEPINOMICS-RES-MAE working group, Roovers J, Djemie T, Barca D, Ceulemans B, Craiu D, Lemke JR, Korff C, Mefford HC, Meyers CT, Siegler Z, Hiatt SM, Cooper GM, Bebin EM, Snijders Blok L, Veenstra-Knol HE, Baugh EH, Brilstra EH, Volker-Touw CML, van Binsbergen E, Revah-Politi A, Pereira E, McBrian D, Pacault M, Isidor B, Le Caignec C, Gilbert-Dussardier B, Bilan F, Heinzen EL, Goldstein DB, Stevens SJC, Sands TT.

Ann Neurol. 2018 Nov;84(5):788-795. doi: 10.1002/ana.25350. Epub 2018 Oct 25.

PMID:
30269351
7.

A triad of infantile spasms, nystagmus and a focal tonic seizure.

Tarodo SG, Nguyen T, Ranza E, Vulliémoz S, Korff CM.

Epileptic Disord. 2018 Aug 1;20(4):295-300. doi: 10.1684/epd.2018.0984.

PMID:
30063026
8.

Desaturation During Cry in the Neonatal Period.

Salomon C, Anastaze Stelle K, Korff CM, Leuchter I, Toso S, Corbelli R, Barazzone Argiroffo C, Ruchonnet-Métrailler I.

Glob Pediatr Health. 2018 Mar 16;5:2333794X18764515. doi: 10.1177/2333794X18764515. eCollection 2018. No abstract available.

9.

Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis.

Knaus A, Pantel JT, Pendziwiat M, Hajjir N, Zhao M, Hsieh TC, Schubach M, Gurovich Y, Fleischer N, Jäger M, Köhler S, Muhle H, Korff C, Møller RS, Bayat A, Calvas P, Chassaing N, Warren H, Skinner S, Louie R, Evers C, Bohn M, Christen HJ, van den Born M, Obersztyn E, Charzewska A, Endziniene M, Kortüm F, Brown N, Robinson PN, Schelhaas HJ, Weber Y, Helbig I, Mundlos S, Horn D, Krawitz PM.

Genome Med. 2018 Jan 9;10(1):3. doi: 10.1186/s13073-017-0510-5.

10.

Circulating neural antibodies in unselected children with new-onset seizures.

Garcia-Tarodo S, Datta AN, Ramelli GP, Maréchal-Rouiller F, Bien CG, Korff CM.

Eur J Paediatr Neurol. 2018 May;22(3):396-403. doi: 10.1016/j.ejpn.2017.12.007. Epub 2017 Dec 21.

PMID:
29291919
11.

FGF4 retrogene on CFA12 is responsible for chondrodystrophy and intervertebral disc disease in dogs.

Brown EA, Dickinson PJ, Mansour T, Sturges BK, Aguilar M, Young AE, Korff C, Lind J, Ettinger CL, Varon S, Pollard R, Brown CT, Raudsepp T, Bannasch DL.

Proc Natl Acad Sci U S A. 2017 Oct 24;114(43):11476-11481. doi: 10.1073/pnas.1709082114. Epub 2017 Oct 11.

12.

Focal cortical malformations in children with early infantile epilepsy and PCDH19 mutations: case report.

Kurian M, Korff CM, Ranza E, Bernasconi A, Lübbig A, Nangia S, Ramelli GP, Wohlrab G, Nordli DR Jr, Bast T.

Dev Med Child Neurol. 2018 Jan;60(1):100-105. doi: 10.1111/dmcn.13595. Epub 2017 Oct 24.

13.

Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.

Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, Tzadok M, Korff C, Dubois F, Ramsey K, Narayanan V, Serratosa JM, Giraldez BG, Helbig I, Marsh E, O'Brien M, Bergqvist CA, Binelli A, Porter B, Zaeyen E, Horovitz DD, Wolff M, Marjanovic D, Caglayan HS, Arslan M, Pena SDJ, Sisodiya SM, Balestrini S, Syrbe S, Veggiotti P, Lemke JR, Møller RS, Lerche H, Rubboli G.

Brain. 2017 Sep 1;140(9):2337-2354. doi: 10.1093/brain/awx184.

PMID:
29050392
14.

What to do in failed hemispherotomy? Our clinical series and review of the literature.

Bartoli A, El Hassani Y, Jenny B, Momjian S, Korff CM, Seeck M, Vulliemoz S, Schaller K.

Neurosurg Rev. 2018 Jan;41(1):125-132. doi: 10.1007/s10143-017-0888-y. Epub 2017 Aug 10. Review.

PMID:
28799142
15.

The Immune System in Pediatric Seizures and Epilepsies.

Korff CM, Dale RC.

Pediatrics. 2017 Sep;140(3). pii: e20163534. doi: 10.1542/peds.2016-3534. Epub 2017 Aug 9. Review.

16.

Drug-Level Monitoring on Admission for Presurgical Epilepsy Evaluation.

Constantinescu I, Korff CM, Vulliemoz S, Picard F, Seeck M.

Eur Neurol. 2017;78(1-2):105-110. doi: 10.1159/000479003. Epub 2017 Jul 24.

PMID:
28738370
17.

SERPINI1 pathogenic variants: An emerging cause of childhood-onset progressive myoclonic epilepsy.

Ranza E, Garcia-Tarodo S, Varvagiannis K, Guipponi M, Lobrinus JA, Bottani A, Kern I, Kurian M, Pittet MP, Antonarakis SE, Fluss J, Korff CM.

Am J Med Genet A. 2017 Sep;173(9):2456-2460. doi: 10.1002/ajmg.a.38317. Epub 2017 Jun 20.

PMID:
28631894
18.

GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.

Platzer K, Yuan H, Schütz H, Winschel A, Chen W, Hu C, Kusumoto H, Heyne HO, Helbig KL, Tang S, Willing MC, Tinkle BT, Adams DJ, Depienne C, Keren B, Mignot C, Frengen E, Strømme P, Biskup S, Döcker D, Strom TM, Mefford HC, Myers CT, Muir AM, LaCroix A, Sadleir L, Scheffer IE, Brilstra E, van Haelst MM, van der Smagt JJ, Bok LA, Møller RS, Jensen UB, Millichap JJ, Berg AT, Goldberg EM, De Bie I, Fox S, Major P, Jones JR, Zackai EH, Abou Jamra R, Rolfs A, Leventer RJ, Lawson JA, Roscioli T, Jansen FE, Ranza E, Korff CM, Lehesjoki AE, Courage C, Linnankivi T, Smith DR, Stanley C, Mintz M, McKnight D, Decker A, Tan WH, Tarnopolsky MA, Brady LI, Wolff M, Dondit L, Pedro HF, Parisotto SE, Jones KL, Patel AD, Franz DN, Vanzo R, Marco E, Ranells JD, Di Donato N, Dobyns WB, Laube B, Traynelis SF, Lemke JR.

J Med Genet. 2017 Jul;54(7):460-470. doi: 10.1136/jmedgenet-2016-104509. Epub 2017 Apr 4.

19.

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.

Depienne C, Nava C, Keren B, Heide S, Rastetter A, Passemard S, Chantot-Bastaraud S, Moutard ML, Agrawal PB, VanNoy G, Stoler JM, Amor DJ, Billette de Villemeur T, Doummar D, Alby C, Cormier-Daire V, Garel C, Marzin P, Scheidecker S, de Saint-Martin A, Hirsch E, Korff C, Bottani A, Faivre L, Verloes A, Orzechowski C, Burglen L, Leheup B, Roume J, Andrieux J, Sheth F, Datar C, Parker MJ, Pasquier L, Odent S, Naudion S, Delrue MA, Le Caignec C, Vincent M, Isidor B, Renaldo F, Stewart F, Toutain A, Koehler U, Häckl B, von Stülpnagel C, Kluger G, Møller RS, Pal D, Jonson T, Soller M, Verbeek NE, van Haelst MM, de Kovel C, Koeleman B, Monroe G, van Haaften G; DDD Study, Attié-Bitach T, Boutaud L, Héron D, Mignot C.

Hum Genet. 2017 Apr;136(4):463-479. doi: 10.1007/s00439-017-1772-0. Epub 2017 Mar 10.

20.

An epidemic of dystonic reactions in central Africa.

Peyraud N, Rafael F, Parker LA, Quere M, Alcoba G, Korff C, Deats M, Esteve PB, Cabrol JC, Serafini M, Ciglenecki I, Rull M, Larabi IA, Baud F, Grandesso F, Ilunga BK, Alvarez JC, Newton PN.

Lancet Glob Health. 2017 Feb;5(2):e137-e138. doi: 10.1016/S2214-109X(16)30287-X. No abstract available.

21.
22.

Serum levels of innate immunity cytokines are elevated in dogs with metaphyseal osteopathy (hypertrophic osteodytrophy) during active disease and remission.

Safra N, Hitchens PL, Maverakis E, Mitra A, Korff C, Johnson E, Kol A, Bannasch MJ, Pedersen NC, Bannasch DL.

Vet Immunol Immunopathol. 2016 Oct 15;179:32-5. doi: 10.1016/j.vetimm.2016.08.003. Epub 2016 Aug 3.

23.

Epileptic spasms in epilepsy with myoclonic-atonic seizures (Doose syndrome).

Pittau F, Korff CM, Nordli DR Jr.

Epileptic Disord. 2016 Sep 1;18(3):289-96. doi: 10.1684/epd.2016.0854.

24.

Epileptic networks are strongly connected with and without the effects of interictal discharges.

Iannotti GR, Grouiller F, Centeno M, Carmichael DW, Abela E, Wiest R, Korff C, Seeck M, Michel C, Pittau F, Vulliemoz S.

Epilepsia. 2016 Jul;57(7):1086-96. doi: 10.1111/epi.13400. Epub 2016 May 6.

25.

Pediatric epilepsy surgery: could age be a predictor of outcomes?

Jenny B, Smoll N, El Hassani Y, Momjian S, Pollo C, Korff CM, Seeck M, Schaller K.

J Neurosurg Pediatr. 2016 Aug;18(2):235-41. doi: 10.3171/2015.10.PEDS14413. Epub 2016 Apr 29.

PMID:
27128787
26.

Diabetic Striatopathy in Childhood: A Case Report.

Faundez T, Klee P, Hanquinet S, Schwitzgebel V, Burkhard PR, Korff CM.

Pediatrics. 2016 Apr;137(4). pii: e20143761. doi: 10.1542/peds.2014-3761. Epub 2016 Mar 24. Erratum in: Pediatrics. 2016 Jul;138(1):.

27.

Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy.

Mignot C, von Stülpnagel C, Nava C, Ville D, Sanlaville D, Lesca G, Rastetter A, Gachet B, Marie Y, Korenke GC, Borggraefe I, Hoffmann-Zacharska D, Szczepanik E, Rudzka-Dybała M, Yiş U, Çağlayan H, Isapof A, Marey I, Panagiotakaki E, Korff C, Rossier E, Riess A, Beck-Woedl S, Rauch A, Zweier C, Hoyer J, Reis A, Mironov M, Bobylova M, Mukhin K, Hernandez-Hernandez L, Maher B, Sisodiya S, Kuhn M, Glaeser D, Weckhuysen S, Myers CT, Mefford HC, Hörtnagel K, Biskup S; EuroEPINOMICS-RES MAE working group, Lemke JR, Héron D, Kluger G, Depienne C.

J Med Genet. 2016 Aug;53(8):511-22. doi: 10.1136/jmedgenet-2015-103451. Epub 2016 Mar 17. Erratum in: J Med Genet. 2016 Oct;53(10):720.

PMID:
26989088
28.

Clinical Variability of GLUT1DS.

Melnikova AM, Korff CM.

Pediatr Neurol Briefs. 2015 Feb;29(2):14. doi: 10.15844/pedneurbriefs-29-2-5.

29.

Vaccinations and Dravet Syndrome.

Korff CM.

Pediatr Neurol Briefs. 2015 Nov;29(11):85. doi: 10.15844/pedneurbriefs-29-11-4.

30.

Effectiveness of antiepileptic therapy in patients with PCDH19 mutations.

Lotte J, Bast T, Borusiak P, Coppola A, Cross JH, Dimova P, Fogarasi A, Graneß I, Guerrini R, Hjalgrim H, Keimer R, Korff CM, Kurlemann G, Leiz S, Linder-Lucht M, Loddenkemper T, Makowski C, Mühe C, Nicolai J, Nikanorova M, Pellacani S, Philip S, Ruf S, Sánchez Fernández I, Schlachter K, Striano P, Sukhudyan B, Valcheva D, Vermeulen RJ, Weisbrod T, Wilken B, Wolf P, Kluger G.

Seizure. 2016 Feb;35:106-10. doi: 10.1016/j.seizure.2016.01.006. Epub 2016 Jan 6.

31.

Successful treatment of neonatal atypical hemolytic uremic syndrome with C5 monoclonal antibody.

Anastaze Stelle K, Gonzalez E, Wilhelm-Bals A, Michelet PR, Korff CM, Parvex P.

Arch Pediatr. 2016 Mar;23(3):283-6. doi: 10.1016/j.arcped.2015.11.020. Epub 2016 Jan 8.

PMID:
26775886
32.

Combined VIth and VIIth nerve palsy: Consider idiopathic intracranial hypertension!

Soroken C, Lacroix L, Korff CM.

Eur J Paediatr Neurol. 2016 Mar;20(2):336-338. doi: 10.1016/j.ejpn.2015.11.007. Epub 2015 Dec 2.

PMID:
26653361
33.

Editorial commentary on "Refractory absence seizures: An Italian multicenter retrospective study" by E. Franzoni et al.

Korff C.

Eur J Paediatr Neurol. 2015 Nov;19(6):617-8. doi: 10.1016/j.ejpn.2015.08.007. Epub 2015 Sep 2. No abstract available.

PMID:
26361849
34.

Epileptic activity is a surrogate for an underlying etiology and stopping the activity has a limited impact on developmental outcome.

Korff CM, Brunklaus A, Zuberi SM.

Epilepsia. 2015 Oct;56(10):1477-81. doi: 10.1111/epi.13105. Epub 2015 Aug 21.

35.

Riboflavin in cyclic vomiting syndrome: efficacy in three children.

Martinez-Esteve Melnikova A, Schäppi MG, Korff C.

Eur J Pediatr. 2016 Jan;175(1):131-5. doi: 10.1007/s00431-015-2597-2. Epub 2015 Jul 31.

PMID:
26226892
36.

A practical, simple, and useful method of categorizing interictal EEG features in children.

Kim SH, Korff CM, Kim AJ, Nordli DR Jr.

Neurology. 2015 Aug 4;85(5):471-8. doi: 10.1212/WNL.0000000000001805. Epub 2015 Jul 2.

37.

Yield of MRI, high-density electric source imaging (HD-ESI), SPECT and PET in epilepsy surgery candidates.

Lascano AM, Perneger T, Vulliemoz S, Spinelli L, Garibotto V, Korff CM, Vargas MI, Michel CM, Seeck M.

Clin Neurophysiol. 2016 Jan;127(1):150-155. doi: 10.1016/j.clinph.2015.03.025. Epub 2015 May 9.

PMID:
26021550
38.

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.

Syrbe S, Hedrich UBS, Riesch E, Djémié T, Müller S, Møller RS, Maher B, Hernandez-Hernandez L, Synofzik M, Caglayan HS, Arslan M, Serratosa JM, Nothnagel M, May P, Krause R, Löffler H, Detert K, Dorn T, Vogt H, Krämer G, Schöls L, Mullis PE, Linnankivi T, Lehesjoki AE, Sterbova K, Craiu DC, Hoffman-Zacharska D, Korff CM, Weber YG, Steinlin M, Gallati S, Bertsche A, Bernhard MK, Merkenschlager A, Kiess W; EuroEPINOMICS RES consortium, Gonzalez M, Züchner S, Palotie A, Suls A, De Jonghe P, Helbig I, Biskup S, Wolff M, Maljevic S, Schüle R, Sisodiya SM, Weckhuysen S, Lerche H, Lemke JR.

Nat Genet. 2015 Apr;47(4):393-399. doi: 10.1038/ng.3239. Epub 2015 Mar 9.

39.

A child with ictal vocalizations and generalized epilepsy.

Kurian M, Heritier Barras AC, Korff CM.

Epileptic Disord. 2015 Mar;17(1):67-70; quiz 71. doi: 10.1684/epd.2015.0727.

40.

Widespread intracranial calcifications in the follow-up of a patient with cartilage-hair hypoplasia--anauxetic dysplasia spectrum disorder: a coincidental finding?

Garcia-Tarodo S, Bottani A, Merlini L, Kaelin A, Schwitzgebel VM, Parvex P, Dayer R, Lascombes P, Korff CM.

Eur J Paediatr Neurol. 2015 May;19(3):367-71. doi: 10.1016/j.ejpn.2014.12.016. Epub 2015 Jan 3.

PMID:
25596067
41.

Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.

Delcourt M, Riant F, Mancini J, Milh M, Navarro V, Roze E, Humbertclaude V, Korff C, Des Portes V, Szepetowski P, Doummar D, Echenne B, Quintin S, Leboucq N, Singh Amrathlal R, Rochette J, Roubertie A.

J Neurol Neurosurg Psychiatry. 2015 Jul;86(7):782-5. doi: 10.1136/jnnp-2014-309025. Epub 2015 Jan 16.

PMID:
25595153
42.

When should clinicians search for GLUT1 deficiency syndrome in childhood generalized epilepsies?

Lebon S, Suarez P, Alija S, Korff CM, Fluss J, Mercati D, Datta AN, Poloni C, Marcoz JP, Campos-Xavier AB, Bonafé L, Roulet-Perez E.

Eur J Paediatr Neurol. 2015 Mar;19(2):170-5. doi: 10.1016/j.ejpn.2014.11.009. Epub 2014 Dec 11.

PMID:
25532859
43.

Autoimmunity and inflammation in status epilepticus: from concepts to therapies.

Holzer FJ, Seeck M, Korff CM.

Expert Rev Neurother. 2014 Oct;14(10):1181-202. doi: 10.1586/14737175.2014.956457. Epub 2014 Sep 9. Review.

PMID:
25201402
44.

Towards the identification of a genetic basis for Landau-Kleffner syndrome.

Conroy J, McGettigan PA, McCreary D, Shah N, Collins K, Parry-Fielder B, Moran M, Hanrahan D, Deonna TW, Korff CM, Webb D, Ennis S, Lynch SA, King MD.

Epilepsia. 2014 Jun;55(6):858-65. doi: 10.1111/epi.12645. Epub 2014 May 14.

45.

Epilepsy: old syndromes, new genes.

Weckhuysen S, Korff CM.

Curr Neurol Neurosci Rep. 2014 Jun;14(6):447. doi: 10.1007/s11910-014-0447-7. Review.

PMID:
24740805
46.

When is a child with status epilepticus likely to have Dravet syndrome?

Le Gal F, Lebon S, Ramelli GP, Datta AN, Mercati D, Maier O, Combescure C, Rodriguez MI, Seeck M, Roulet E, Korff CM.

Epilepsy Res. 2014 May;108(4):740-7. doi: 10.1016/j.eplepsyres.2014.02.019. Epub 2014 Mar 12.

PMID:
24679980
47.

Localization of the epileptogenic tuber with electric source imaging in patients with tuberous sclerosis.

Kargiotis O, Lascano AM, Garibotto V, Spinelli L, Genetti M, Wissmeyer M, Korff CM, Momjian S, Michel CM, Seeck M, Vulliemoz S.

Epilepsy Res. 2014 Feb;108(2):267-79. doi: 10.1016/j.eplepsyres.2013.11.003. Epub 2013 Nov 19.

PMID:
24315017
48.

Positive outcome following early diagnosis and treatment of pyridoxal-5'-phosphate oxidase deficiency: a case report.

Porri S, Fluss J, Plecko B, Paschke E, Korff CM, Kern I.

Neuropediatrics. 2014 Feb;45(1):64-8. doi: 10.1055/s-0033-1353489. Epub 2013 Sep 25.

PMID:
24297574
49.

Early-onset or rapidly progressive scoliosis in children: check the eyes!

Kurian M, Megevand C, De Haller R, Merlini L, Boex C, Truffert A, Kaelin A, Burglen L, Korff CM.

Eur J Paediatr Neurol. 2013 Nov;17(6):671-5. doi: 10.1016/j.ejpn.2013.05.011. Epub 2013 Jun 28.

PMID:
23810770
50.

Head stereotypies in STXBP1 encephalopathy.

Kim YO, Korff CM, Villaluz MM, Suls A, Weckhuysen S, De Jonghe P, Scheffer IE.

Dev Med Child Neurol. 2013 Aug;55(8):769-72. doi: 10.1111/dmcn.12197. Epub 2013 Jun 13.

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