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Pontocerebellar hypoplasia type 2: variability in clinical and imaging findings.
Eur J Paediatr Neurol. 2007 May;11(3):146-52. doi: 10.1016/j.ejpn.2006.11.012. Epub 2007 Feb 22.
Eur J Paediatr Neurol. 2007.
PMID: 17320436
Cerebral sinus venous thrombosis in Swiss children.
Grunt S, Wingeier K, Wehrli E, Boltshauser E, Capone A, Fluss J, Gubser-Mercati D, Jeannet PY, Keller E, Marcoz JP, Schmitt-Mechelke T, Weber P, Weissert M, Steinlin M; Swiss Neuropaediatric Stroke Registry.
Grunt S, et al. Among authors: gubser mercati d.
Dev Med Child Neurol. 2010 Dec;52(12):1145-50. doi: 10.1111/j.1469-8749.2010.03722.x.
Dev Med Child Neurol. 2010.
PMID: 20573178
Free article.
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The first three years of the Swiss Neuropaediatric Stroke Registry (SNPSR): a population-based study of incidence, symptoms and risk factors.
Steinlin M, Pfister I, Pavlovic J, Everts R, Boltshauser E, Capone Mori A, Gubser Mercati D, Hänggeli CA, Keller E, Luetschg J, Marcoz J, Ramelli GP, Roulet Perez E, Schmitt-Mechelke T, Weissert M; Swiss Societies of Paediatric Neurology and Neonatology.
Steinlin M, et al. Among authors: gubser mercati d.
Neuropediatrics. 2005 Apr;36(2):90-7. doi: 10.1055/s-2005-837658.
Neuropediatrics. 2005.
PMID: 15822021
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Neuropsychological problems after paediatric stroke: two year follow-up of Swiss children.
Pavlovic J, Kaufmann F, Boltshauser E, Capone Mori A, Gubser Mercati D, Haenggeli CA, Keller E, Lütschg J, Marcoz JP, Ramelli GP, Roulet Perez E, Schmitt-Mechelke T, Weissert M, Steinlin M.
Pavlovic J, et al. Among authors: gubser mercati d.
Neuropediatrics. 2006 Feb;37(1):13-9. doi: 10.1055/s-2006-923932.
Neuropediatrics. 2006.
PMID: 16541363
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Delayed diagnosis of acute ischemic stroke in children - a registry-based study in Switzerland.
Martin C, von Elm E, El-Koussy M, Boltshauser E, Steinlin M; Swiss Neuropediatric Stroke Registry study group.
Martin C, et al.
Swiss Med Wkly. 2011 Oct 19;141:w13281. doi: 10.4414/smw.2011.13281. eCollection 2011.
Swiss Med Wkly. 2011.
PMID: 22012483
Free article.
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Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
Laugel V, Dalloz C, Durand M, Sauvanaud F, Kristensen U, Vincent MC, Pasquier L, Odent S, Cormier-Daire V, Gener B, Tobias ES, Tolmie JL, Martin-Coignard D, Drouin-Garraud V, Heron D, Journel H, Raffo E, Vigneron J, Lyonnet S, Murday V, Gubser-Mercati D, Funalot B, Brueton L, Sanchez Del Pozo J, Muñoz E, Gennery AR, Salih M, Noruzinia M, Prescott K, Ramos L, Stark Z, Fieggen K, Chabrol B, Sarda P, Edery P, Bloch-Zupan A, Fawcett H, Pham D, Egly JM, Lehmann AR, Sarasin A, Dollfus H.
Laugel V, et al. Among authors: gubser mercati d.
Hum Mutat. 2010 Feb;31(2):113-26. doi: 10.1002/humu.21154.
Hum Mutat. 2010.
PMID: 19894250
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[Management of the handicapped child. Summary of a psychosocial workshop].
Gubser-Mercati D, De Meuron G.
Gubser-Mercati D, et al.
Rev Med Suisse Romande. 1997 Oct;117(10):759-61.
Rev Med Suisse Romande. 1997.
PMID: 9441356
French.
No abstract available.
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