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Helle Hjalgrim

Showing results (11-20 of 71) with videos related to

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Ugeskrift for Laeger|September 3, 2008
[Clinical aspects of Tourette syndrome]Nanette M M Mol Debes, Helle Hjalgrim, Liselotte Skov
Journal of Child Neurology|October 2, 2008
Validation of the presence of comorbidities in a Danish clinical cohort of children with Tourette syndromeNanette M M Mol Debes, Helle Hjalgrim, Liselotte Skov
Epilepsy Research|June 20, 2020
The clinical spectrum of familial and sporadic idiopathic generalized epilepsyJoanna Gesche, Helle Hjalgrim, Guido Rubboli, et al.
Epilepsy Research|January 9, 2021
Risk factors of paradoxical reactions to anti-seizure medication in genetic generalized epilepsyJoanna Gesche, Helle Hjalgrim, Guido Rubboli, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
A nonsense mutation in FMR1 causing fragile X syndromeKaren Grønskov, Karen Brøndum-Nielsen, Alma Dedic, et al.
Ugeskrift for Laeger|September 3, 2008
[Tourette syndrome. Genetics, neuroanatomy and neurotransmitters]Nanette M M Mol Debes, Liselotte Skov, Helle Hjalgrim
Neurology|August 21, 2020
Patterns and prognostic markers for treatment response in generalized epilepsiesJoanna Gesche, Helle Hjalgrim, Guido Rubboli, et al.
Ugeskrift for Laeger|October 30, 2014
[Glucose transporter-1 deficiency syndrome can cause various clinical symptoms]Jan Larsen, Vibeke Stubbings, Rikke Steensbjerre Møller, et al.
Lancet (London, England)|April 20, 2002
Absence of nasal bone and detection of trisomy 21Helle Hjalgrim, Johanne M Hahnemann, Inger Kjaer, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
9q Subtelomeric deletion syndrome with diaphragmatic herniaLaura L Klitten, Niels Tommerup, Helle Hjalgrim, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
Ugeskrift for Laeger|September 3, 2008
[Clinical aspects of Tourette syndrome]Nanette M M Mol Debes, Helle Hjalgrim, Liselotte Skov
Journal of Child Neurology|October 2, 2008
Validation of the presence of comorbidities in a Danish clinical cohort of children with Tourette syndromeNanette M M Mol Debes, Helle Hjalgrim, Liselotte Skov
Epilepsy Research|June 20, 2020
The clinical spectrum of familial and sporadic idiopathic generalized epilepsyJoanna Gesche, Helle Hjalgrim, Guido Rubboli, et al.
Epilepsy Research|January 9, 2021
Risk factors of paradoxical reactions to anti-seizure medication in genetic generalized epilepsyJoanna Gesche, Helle Hjalgrim, Guido Rubboli, et al.
European Journal of Human Genetics : EJHG|January 27, 2011
A nonsense mutation in FMR1 causing fragile X syndromeKaren Grønskov, Karen Brøndum-Nielsen, Alma Dedic, et al.
Ugeskrift for Laeger|September 3, 2008
[Tourette syndrome. Genetics, neuroanatomy and neurotransmitters]Nanette M M Mol Debes, Liselotte Skov, Helle Hjalgrim
Neurology|August 21, 2020
Patterns and prognostic markers for treatment response in generalized epilepsiesJoanna Gesche, Helle Hjalgrim, Guido Rubboli, et al.
Ugeskrift for Laeger|October 30, 2014
[Glucose transporter-1 deficiency syndrome can cause various clinical symptoms]Jan Larsen, Vibeke Stubbings, Rikke Steensbjerre Møller, et al.
Lancet (London, England)|April 20, 2002
Absence of nasal bone and detection of trisomy 21Helle Hjalgrim, Johanne M Hahnemann, Inger Kjaer, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
9q Subtelomeric deletion syndrome with diaphragmatic herniaLaura L Klitten, Niels Tommerup, Helle Hjalgrim, et al.
Pageof 8