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Gallenmüller, Constanze
25  Ergebnisse:
Personensuche X
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1

Mast Syndrome Outside the Amish Community: SPG21 in Europe:

Amprosi, Matthias ; Indelicato, Elisabetta ; Nachbauer, Wolfgang...
Frontiers in Neurology.  12 (2022)  - p. , 2022
Link: https://doi.org/10.3389/..
 
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2

Smoking and alcohol, health-related quality of life and psy..:

Rabenstein, Andrea ; Catarino, Claudia B. ; Rampeltshammer, Verena...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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3

Brain diffusion tensor imaging changes in cerebrotendinous ..:

Catarino, Claudia B. ; Vollmar, Christian ; Küpper, Clemens...
Journal of Neurology.  265 (2017)  2 - p. 388-393 , 2017
Link: https://doi.org/10.1007/..
 
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4

Idebenone Is Effective and Well Tolerated in Leber's Heredi..:

Klopstock, Thomas ; Metz, Guenther ; Gallenmüller, Constanze...
Neurology.  86 (2016)  16_supplement - p. , 2016
Link: https://doi.org/10.1212/..
 
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5

SYNE1 ataxia is a common recessive ataxia with major non-ce..:

Synofzik, Matthis ; Smets, Katrien ; Mallaret, Martial...
Brain.  139 (2016)  5 - p. 1378-1393 , 2016
Link: https://doi.org/10.1093/..
 
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6

Hereditary spastic paraplegia: Clinicogenetic lessons from ..:

Schüle, Rebecca ; Wiethoff, Sarah ; Martus, Peter...
Annals of Neurology.  79 (2016)  4 - p. 646-658 , 2016
Link: https://doi.org/10.1002/..
 
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7

MRPL44 mutations cause a slowly progressive multisystem dis..:

Distelmaier, Felix ; Haack, Tobias B. ; Catarino, Claudia B....
neurogenetics.  16 (2015)  4 - p. 319-323 , 2015
Link: https://doi.org/10.1007/..
 
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8

Paranoid delusion as lead symptom in two siblings with late..:

Stendel, Claudia ; Gallenmüller, Constanze ; Peters, Katrin...
Journal of Neurology.  262 (2015)  4 - p. 1072-1073 , 2015
Link: https://doi.org/10.1007/..
 
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9

Novel phenotype associated with a mutation in the KCNA1(Kv1..:

D'Adamo, Maria C. ; Gallenmüller, Constanze ; Servettini, Ilenio...
Frontiers in Physiology.  5 (2015)  - p. , 2015
Link: https://doi.org/10.3389/..
 
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10

Novel ATM mutation in a German patient presenting as genera..:

Kuhm, Christoph ; Gallenmüller, Constanze ; Dörk, Thilo...
Journal of Neurology.  262 (2015)  3 - p. 768-770 , 2015
Link: https://doi.org/10.1007/..
 
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11

Molekulargenetische Analyse bei Patienten mit kongenitalen .. 

Untersuchung von seltenen Krankheitsgenen und von Kandidate... 
Gallenmüller, Constanze , 2014
Link: http://nbn-resolving.de/..
 
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12

Salbutamol-responsive limb-girdle congenital myasthenic syn..:

Gallenmüller, Constanze ; Müller-Felber, Wolfgang ; Dusl, Marina...
Neuromuscular Disorders.  24 (2014)  1 - p. 31-35 , 2014
Link: https://doi.org/10.1016/..
 
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13

Idebenone treatment for Leber hereditary optic neuropathy —..:

Yu-Wai-Man, Patrick ; Klopstock, Thomas ; Metz, Günther...
Mitochondrion.  13 (2013)  6 - p. 901 , 2013
Link: https://doi.org/10.1016/..
 
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14

Congenital myasthenic syndromes: Achievements and limitatio..:

Abicht, Angela ; Dusl, Marina ; Gallenmüller, Constanze...
Human Mutation.  33 (2012)  10 - p. 1474-1484 , 2012
Link: https://doi.org/10.1002/..
 
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15

Mast Syndrome Outside the Amish Community: SPG21 in Europe:

Amprosi, Matthias ; Indelicato, Elisabetta ; Nachbauer, Wolfgang...
info:eu-repo/semantics/altIdentifier/pmid/pmid:35111129.  , 2022
Link: https://pub.dzne.de/reco..
 
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