Search research articles
Contact Us
Filters
Showing results (181-190 of 197) with videos related to
Page
of 20
Sort By:
Cephalalgia : an International Journal of Headache
|
February 18, 2009
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy
M-J Castro, A H Stam, C Lemos, et al.
Breast Cancer Research and Treatment
|
April 17, 2016
Sentinel lymph node biopsy can be omitted in DCIS patients treated with breast conserving therapy
L M van Roozendaal, B Goorts, M Klinkert, et al.
European Journal of Cancer (Oxford, England : 1990)
|
July 16, 2013
Doxorubicin/cyclophosphamide with concurrent versus sequential docetaxel as neoadjuvant treatment in patients with breast cancer
B E P J Vriens, M J B Aarts, B de Vries, et al.
Early Human Development
|
February 8, 2024
Role of patent ductus arteriosus in preterms in long-term outcome
Moniek S Veldhuis, Laura M L Dix, Johannes M P J Breur, et al.
Cephalalgia : an International Journal of Headache
|
May 24, 2008
CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood
B de Vries, A H Stam, F Beker, et al.
Clinical Radiology
|
October 15, 2017
Diagnostic performance of gadofosveset-enhanced axillary MRI for nodal (re)staging in breast cancer patients: results of a validation study
T J A van Nijnatten, R J Schipper, M B I Lobbes, et al.
Neurology
|
January 15, 2010
Shared genetic factors in migraine and depression: evidence from a genetic isolate
A H Stam, B de Vries, A C J W Janssens, et al.
Journal of Medical Genetics
|
March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
B B de Vries, S M White, S J Knight, et al.
Clinical Genetics
|
November 22, 2007
Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes
M-J Castro, B Nunes, B de Vries, et al.
Journal of Medical Genetics
|
February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects
Marjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 197) with videos related to
Sort By:
Page
of 20
Cephalalgia : an International Journal of Headache
|
February 18, 2009
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy
M-J Castro, A H Stam, C Lemos, et al.
Breast Cancer Research and Treatment
|
April 17, 2016
Sentinel lymph node biopsy can be omitted in DCIS patients treated with breast conserving therapy
L M van Roozendaal, B Goorts, M Klinkert, et al.
European Journal of Cancer (Oxford, England : 1990)
|
July 16, 2013
Doxorubicin/cyclophosphamide with concurrent versus sequential docetaxel as neoadjuvant treatment in patients with breast cancer
B E P J Vriens, M J B Aarts, B de Vries, et al.
Early Human Development
|
February 8, 2024
Role of patent ductus arteriosus in preterms in long-term outcome
Moniek S Veldhuis, Laura M L Dix, Johannes M P J Breur, et al.
Cephalalgia : an International Journal of Headache
|
May 24, 2008
CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood
B de Vries, A H Stam, F Beker, et al.
Clinical Radiology
|
October 15, 2017
Diagnostic performance of gadofosveset-enhanced axillary MRI for nodal (re)staging in breast cancer patients: results of a validation study
T J A van Nijnatten, R J Schipper, M B I Lobbes, et al.
Neurology
|
January 15, 2010
Shared genetic factors in migraine and depression: evidence from a genetic isolate
A H Stam, B de Vries, A C J W Janssens, et al.
Journal of Medical Genetics
|
March 10, 2001
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
B B de Vries, S M White, S J Knight, et al.
Clinical Genetics
|
November 22, 2007
Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes
M-J Castro, B Nunes, B de Vries, et al.
Journal of Medical Genetics
|
February 28, 2012
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects
Marjolein H Willemsen, Lisenka E L Vissers, Michèl A A P Willemsen, et al.
Page
of 20