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Publications by Evangelista, Teresinha

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Number of items: 4.

Journal article

McMacken, Grace; Whittaker, Roger G.; Evangelista, Teresinha; Abicht, Angela; Dusl, Marina; Lochmüller, Hanns (2018): Congenital myasthenic syndrome with episodic apnoea: clinical, neurophysiological and genetic features in the long-term follow-up of 19 patients. In: Journal of Neurology, Vol. 265, No. 1: pp. 194-203

Owen, David; Topf, Ana; Preethish-Kumar, Veeramani; Lorenzoni, Paulo Jose; Vroling, Bas; Scola, Rosana Herminia; Dias-Tosta, Elza; Geraldo, Argemiro; Polavarapu, Kiran; Nashi, Saraswati; Cox, Daniel; Evangelista, Teresinha; Dawson, John; Thompson, Rachel; Senderek, Jan; Laurie, Steven; Beltran, Sergi; Gut, Marta; Gut, Ivo; Nalini, Atchayaram; Lochmüller, Hanns (2018): Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness. In: American Journal of Medical Genetics Part A, Vol. 176, No. 7: pp. 1594-1601

Lukacs, Zoltan; Cobos, Paulina Nieves; Wenninger, Stephan; Willis, Tracey A.; Guglieri, Michela; Roberts, Marc; Quinlivan, Rosaline; Hilton-Jones, David; Evangelista, Teresinha; Zierz, Stephan; Schlotter-Weigel, Beate; Walter, Maggie C.; Reilich, Peter; Klopstock, Thomas; Deschauer, Marcus; Straub, Volker; Müller-Felber, Wolfgang; Schoser, Benedikt (2016): Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness. In: Neurology, Vol. 87, No. 3: pp. 295-298

O'Connor, Emily; Töpf, Ana; Müller, Juliane S.; Cox, Daniel; Evangelista, Teresinha; Colomer, Jaume; Abicht, Angela; Senderek, Jan; Hasselmann, Oswald; Yaramis, Ahmet; Laval, Steven H.; Lochmüller, Hanns (2016): Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome. In: Brain, Vol. 139: pp. 2143-2153

This list was generated on Sat Sep 21 16:27:31 2019 CEST.