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Current Neurology and Neuroscience Reports
|
August 22, 2013
Episodic movement disorders: from phenotype to genotype and back
Knut Brockmann
Developmental Medicine and Child Neurology
|
May 19, 2011
Towards a more palatable treatment for Glut1 deficiency syndrome
Knut Brockmann
Brain & Development
|
March 24, 2009
The expanding phenotype of GLUT1-deficiency syndrome
Knut Brockmann
American Journal of Medical Genetics. Part A
|
September 25, 2023
Moebius syndrome and gastroschisis-The second case of a rare association
Knut Brockmann, Silke Kaulfuß
Archives of Dermatology
|
October 11, 2002
Juvenile horseplay purpura
Knut Brockmann, Katharina Diepold
JAMA Neurology
|
December 3, 2019
Dopamine-Mediated Yawning-Fatigue Syndrome With Specific Recurrent Initiation and Responsiveness to Opioids
Payam Dibaj, Knut Brockmann, Jutta Gärtner
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 27, 2007
Virchow-Robin spaces on magnetic resonance images of children with adrenoleukodystrophy
Samuel Groeschel, Knut Brockmann, Folker Hanefeld
American Journal of Medical Genetics. Part A
|
July 16, 2008
Monozygotic twins discordant for Proteus syndrome
Knut Brockmann, Rudolf Happle, Frank Oeffner, et al.
Neurology. Clinical Practice
|
June 25, 2026
Clinical Differentiation of Self-Limited Epilepsy With Autonomic Seizures (Panayiotopoulos Syndrome) and Childhood Migraine
Eva Berg, Niels K N Focke, Knut Brockmann
Proceedings (Baylor University. Medical Center)
|
December 29, 2022
Hemifacial spasm through changes of cerebrospinal fluid pressure in idiopathic intracranial hypertension
Gabriel Cassinelli Petersen, Mitra Amirkhizi, Knut Brockmann, et al.
Page
of 13
Search research articles
Search
Showing results (1-10 of 125) with videos related to
Sort By:
Page
of 13
Current Neurology and Neuroscience Reports
|
August 22, 2013
Episodic movement disorders: from phenotype to genotype and back
Knut Brockmann
Developmental Medicine and Child Neurology
|
May 19, 2011
Towards a more palatable treatment for Glut1 deficiency syndrome
Knut Brockmann
Brain & Development
|
March 24, 2009
The expanding phenotype of GLUT1-deficiency syndrome
Knut Brockmann
American Journal of Medical Genetics. Part A
|
September 25, 2023
Moebius syndrome and gastroschisis-The second case of a rare association
Knut Brockmann, Silke Kaulfuß
Archives of Dermatology
|
October 11, 2002
Juvenile horseplay purpura
Knut Brockmann, Katharina Diepold
JAMA Neurology
|
December 3, 2019
Dopamine-Mediated Yawning-Fatigue Syndrome With Specific Recurrent Initiation and Responsiveness to Opioids
Payam Dibaj, Knut Brockmann, Jutta Gärtner
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 27, 2007
Virchow-Robin spaces on magnetic resonance images of children with adrenoleukodystrophy
Samuel Groeschel, Knut Brockmann, Folker Hanefeld
American Journal of Medical Genetics. Part A
|
July 16, 2008
Monozygotic twins discordant for Proteus syndrome
Knut Brockmann, Rudolf Happle, Frank Oeffner, et al.
Neurology. Clinical Practice
|
June 25, 2026
Clinical Differentiation of Self-Limited Epilepsy With Autonomic Seizures (Panayiotopoulos Syndrome) and Childhood Migraine
Eva Berg, Niels K N Focke, Knut Brockmann
Proceedings (Baylor University. Medical Center)
|
December 29, 2022
Hemifacial spasm through changes of cerebrospinal fluid pressure in idiopathic intracranial hypertension
Gabriel Cassinelli Petersen, Mitra Amirkhizi, Knut Brockmann, et al.
Page
of 13