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Reinhard Keimer
Observed names:
Keimer, Reinhard,
R Keimer,
R. Keimer
Observed institutions:
University of Bonn,
University Hospital Bonn,
University Medical Center Freiburg,
University Hospital Heidelberg,
Holy Family Hospital Nazareth,
Olgahospital,
Klinikum Stuttgart
show all 7
OpenAlex ID:
A5086469775
Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial
2018
·
Finbar J K O'Callaghan
, Stuart W Edwards
, et al.
·
The Lancet Child & Adolescent Health
·
171
PDF
Effectiveness of antiepileptic therapy in patients with PCDH19 mutations
2016
·
Jan Lotte
, Thomas Bast
, et al.
·
Seizure
·
78
PDF
Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5-related epilepsy
2015
·
A. Müller
, I. Helbig
, et al.
·
European Journal of Paediatric Neurology
·
73
Outcome and predictors of interstitial radiosurgery in the treatment of gelastic epilepsy
2008
·
A. Schulze-Bonhage
, M. Trippel
, et al.
·
Neurology
·
70
Interstitial radiosurgery in the treatment of gelastic epilepsy due to hypothalamic hamartomas
2004
·
A. Schulze-Bonhage
, V. Homberg
, et al.
·
Neurology
·
63
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
2020
·
Holger Hengel
, Célia Bosso-Lefèvre
, et al.
·
Nature Communications
·
57
PDF
Biallelic variants in the transcription factor PAX7 are a new genetic cause of myopathy
2019
·
René G. Feichtinger
, Bettina E. Mucha
, et al.
·
Genetics in Medicine
·
47
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery
2020
·
Holger Hengel
, Rebecca Buchert
, et al.
·
European Journal of Human Genetics
·
40
PDF
GPT2 mutations cause developmental encephalopathy with microcephaly and features of complicated hereditary spastic paraplegia
2018
·
H. Hengel
, R. Keimer
, et al.
·
Clinical Genetics
·
18
A previously identified missense mutation in STYXL1 is likely benign
2018
·
Holger Hengel
, Yvonne Schelling
, et al.
·
European Journal of Medical Genetics
·
2
Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery
2021
·
Holger Hengel
, Rebecca Buchert
, et al.
·
European Journal of Human Genetics
·
1
PDF
Giant Axonal Neuropathy – a neurodegenerative disorder – a novel mutation in the GAN-Gen
2005
·
K Marquard
, B Rautenstrauss
, et al.
·
Neuropediatrics
·
1
Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
2015
·
J. Lotte
, T. Bast
, et al.
·
Neuropediatrics
Central Core Myopathy with Mutation of the RYR1 Gene in Combination with Mutation of the COL6A2 Gene and Severe Infantile Myoclonic Epilepsy
2014
·
T. Weisbrod
, R. Keimer
, et al.
·
Neuropediatrics
Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations
2013
·
A Müller
, T Bast
, et al.
·
Neuropediatrics
Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood
2011
·
S Kirsch
, T von Kalle
, et al.
·
Neuropediatrics
Helmets or physiotherapy? Natural history and treatment options for non-synostotic skull deformity in children – results of a literature search
2010
·
C Reihle
, K Marquard
, et al.
·
Neuropediatrics
Neurofibromatosis type 1 (Recklinghausen's Disease). Who was Friedrich Daniel von Recklinghausen?
2010
·
B Köhler
, R Keimer
·
Neuropediatrics
Efficacy of interstitial radiosurgery in the treatment of pharmacoresistant gelastic epilepsy due to hypothalamic hamartomas
2006
·
A Schulze-Bonhage
, T Bast
, et al.
·
Neuropediatrics
Impact of stereotactic interstitial radiosurgery on cognition in ten juvenile epilepsy patients with hypothalamic hamartoma
2006
·
K Wagner
, L Frings
, et al.
·
Neuropediatrics
Anfallssemiologie bei hypothalamischen Hamartomen
2006
·
Deimling, Florian von
, Bast, Thomas
, et al.
·
FreiDok plus (Universitätsbibliothek Freiburg)
Stiripentol (Diacomit) treatment for child with myoclonic epilepsy in infancy resistant to conventional drugs
2005
·
R Keimer
, K Marquard
, et al.
·
Neuropediatrics
Stereotaktische 123J-Seed-Implantation als Therapieoption pharmakorefraktärer Epilepsien bei hypothalamischen Hamartomen
2003
·
Hömberg, Volker
, Schulze-Bonhage, Andreas
, et al.
·
FreiDok plus (Universitätsbibliothek Freiburg)
Ergebnisse epilepsiechirurgischer Eingriffe bei Kindern mit fokalen corticalen Dysplasien
2003
·
Carmona, Hans
, Schulze-Bonhage, Andreas
, et al.
·
FreiDok plus (Universitätsbibliothek Freiburg)
Stereotactic 125-Seed-Implantation - a possible treatment for refractory epilepsy associated with hypothalamic hamartoma
2002
·
Hömberg, Volker
, Schulze-Bonhage, Andreas
, et al.
·
FreiDok plus (Universitätsbibliothek Freiburg)
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Works count:
27
Citation count:
621
H-index:
9
I10-index:
9
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