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1
Involvement of chromosome 22 in ependymomas
Involvement of chromosome 22 in ependymomas
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Involvement of chromosome 22 in ependymomas

Wernicke, Catrin ; Thiel, Gundula ; Lozanova, Tanka ; Vogel, Siegfried ; Kintzel, Dieter ; Jänisch, Werner ; Lehmann, Karin ; Witkowski, Regine

Cancer genetics and cytogenetics, 1995-02, Vol.79 (2), p.173-176

New York, NY: Elsevier Inc

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2
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias
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A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias

STRUPP, M ; KALLA, R ; LEHMANN-HORN, F ; JURKAT-ROTT, K ; BRANDT, T ; JEN, J. C ; JAHN, K ; CLAASSEN, J ; ADRION, C ; MANSMANN, U ; KLOPSTOCK, T ; FREILINGER, T ; NEUGEBAUER, H ; SPIEGEL, R ; DICHGANS, M

Neurology, 2011-07, Vol.77 (3), p.269-275 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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3
Sodium (23Na) MRI detects elevated muscular sodium concentration in Duchenne muscular dystrophy
Sodium (23Na) MRI detects elevated muscular sodium concentration in Duchenne muscular dystrophy
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Sodium (23Na) MRI detects elevated muscular sodium concentration in Duchenne muscular dystrophy

WEBER, M.-A ; NAGEL, A. M ; JURKAT-ROTT, K ; LEHMANN-HORN, F

Neurology, 2011-12, Vol.77 (23), p.2017-2024 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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4
Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degeneration
Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degeneration
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Permanent muscular sodium overload and persistent muscle edema in Duchenne muscular dystrophy: a possible contributor of progressive muscle degeneration

Weber, M.-A. ; Nagel, A. M. ; Wolf, M. B. ; Jurkat-Rott, K. ; Kauczor, H.-U. ; Semmler, W. ; Lehmann-Horn, F.

Journal of neurology, 2012-11, Vol.259 (11), p.2385-2392 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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5
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants
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Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

JURKAT-ROTT, K ; FREILINGER, T ; DREIER, J. P ; HERZOG, J ; GÖBEL, H ; PETZOLD, G. C ; MONTAGNA, P ; GASSER, T ; LEHMANN-HORN, F ; DICHGANS, M

Neurology, 2004-05, Vol.62 (10), p.1857-1861 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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6
Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12‐q12 in 14 Families
Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12‐q12 in 14 Families
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Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12‐q12 in 14 Families

Weber, Yvonne G. ; Berger, Andrea ; Bebek, Nerses ; Maier, Sabine ; Karafyllakes, Skevos ; Meyer, Nancy ; Fukuyama, Yukio ; Halbach, Anne ; Hikel, Christiane ; Kurlemann, Gerhard ; Neubauer, Bernd ; Osawa, Makiko ; Püst, Burkhard ; Rating, Dietz ; Saito, Kayoko ; Stephani, Ulrich ; Tauer, Ulrike ; Lehmann‐Horn, Frank ; Jurkat‐Rott, Karin ; Lerche, Holger

Epilepsia (Copenhagen), 2004-06, Vol.45 (6), p.601-609 [Periódico revisado por pares]

350 Main Street , Malden , MA 02148 , USA and 9600 Garsington Road , Oxford , OX4 2XG , England: Blackwell Science Inc

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7
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A
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Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A

Sternberg, Damien ; Maisonobe, Thierry ; Jurkat-Rott, Karin ; Nicole, Sophie ; Launay, Erika ; Chauveau, Dominique ; Tabti, Nacira ; Lehmann-Horn, Frank ; Hainque, Bernard ; Fontaine, Bertrand

Brain (London, England : 1878), 2001-06, Vol.124 (6), p.1091-1099 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Andersen-Tawil syndrome : New potassium channel mutations and possible phenotypic variation
Andersen-Tawil syndrome : New potassium channel mutations and possible phenotypic variation
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Andersen-Tawil syndrome : New potassium channel mutations and possible phenotypic variation

DAVIES, N. P ; IMBRICI, P ; GIUNTI, P ; PARSONS, L. M ; THOMAS, M ; MANZUR, A. Y ; JURKAT-ROTT, K ; LEHMANN-HORN, F ; CHINNERY, P. F ; ROSE, M ; KULLMANN, D. M ; HANNA, M. G ; FIALHO, D ; HERD, C ; BILSLAND, L. G ; WEBER, A ; MUELLER, R ; HILTON-JONES, D ; EALING, J ; BOOTHMAN, B. R

Neurology, 2005-10, Vol.65 (7), p.1083-1089 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

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9
Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study
Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study
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Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study

Kassubek, Jan ; Juengling, Freimut D. ; Hoffmann, Stefanie ; Rosenbohm, Angela ; Kurt, Anja ; Jurkat-Rott, Karin ; Steinbach, Peter ; Wolf, Michael ; Ludolph, Albert C. ; Lehmann-Horn, Frank ; Lerche, Holger ; Weber, Yvonne G.

Neuroscience letters, 2003-09, Vol.348 (2), p.73-76 [Periódico revisado por pares]

Shannon: Elsevier Ireland Ltd

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10
Evaluation of Carisbamate for the Treatment of Migraine in a Randomized, Double-Blind Trial
Evaluation of Carisbamate for the Treatment of Migraine in a Randomized, Double-Blind Trial
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Evaluation of Carisbamate for the Treatment of Migraine in a Randomized, Double-Blind Trial

Cady, Roger K. ; Mathew, Ninan ; Diener, Hans-Christoph ; Hu, Peter ; Haas, Magali ; Novak, Gerald P.

Headache, 2009-02, Vol.49 (2), p.216-226 [Periódico revisado por pares]

Malden, USA: Blackwell Publishing Inc

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