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B

Bauer, Juergen and Isojaervi, J. I. T. and Herzog, A. G. and Reuber, M. and Polson, D. and Tauboll, E. and Genton, P. and van der Ven, H. and Roesing, B. and Luef, G. J. and Galimberti, C. A. and van Parys, J. and Fluegel, D. and Bergmann, A. and Elger, C. E. (2002) Reproductive dysfunction in women with epilepsy: recommendations for evaluation and management. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 73 (2). pp. 121-125. ISSN 0022-3050

H

Hehr, Ute and Hehr, A. and Uyanik, G. and Phelan, E. and Winkler, J. and Reardon, W. (2006) A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndrome. JOURNAL OF MEDICAL GENETICS, 43 (6). pp. 541-544. ISSN 0022-2593

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Kleiter, Ingo and Hans, V. H. and Schuierer, Gerhard and Marienhagen, Joerg and Hau, Peter and Schuetz, H. and Bogdahn, Ulrich and Steinbrecher, Andreas (2004) Intraventricular cytarabine in a case of idiopathic hypertrophic pachymeningitis. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 75 (9). pp. 1346-1348. ISSN 0022-3050

Kortuem, Fanny and Das, Soma and Flindt, Max and Morris-Rosendahl, Deborah J. and Stefanova, Irina and Goldstein, Amy and Horn, Denise and Klopocki, Eva and Kluger, Gerhard and Martin, Peter and Rauch, Anita and Roumer, Agathe and Saitta, Sulagna and Walsh, Laurence E. and Wieczorek, Dagmar and Uyanik, Goekhan and Kutsche, Kerstin and Dobyns, William B. (2011) The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. JOURNAL OF MEDICAL GENETICS, 48 (6). pp. 396-406. ISSN 0022-2593

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Luerding, Ralf and Boesebeck, F. and Ebner, A. (2004) Cognitive changes after epilepsy surgery in the posterior cortex. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 75 (4). pp. 583-587. ISSN 0022-3050

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Peinemann, A. and Schuller, S. and Staedtler, M. and Pohl, C. and Jahn, T. and Weindl, A. and Kassubek, J. (2005) Correlation of striatal and insular atrophy with executive dysfunction in early stages of Huntington's disease. In: World Congress on Huntingtons Disease, September 10-13, 2005, Manchester, England.