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Ketil Heimdal

Showing results (21-30 of 52) with videos related to

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Pediatric Pulmonology|September 18, 2024
Tracheobronchomalacia is common in children with primary ciliary dyskinesia-A case note reviewSynne S Kennelly, Vegard Hovland, Iren Lindbak Matthews, et al.
Plos One|July 9, 2015
A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1Irene Johnsrud, Mari Ann Kulseth, Olaug Kristin Rødningen, et al.
Acta Oto-Laryngologica|December 15, 2020
Head and neck paragangliomas in Norway, importance of genetics, updated diagnostic workup and treatmentMohammad Usman Rana, Arild André Østhus, Ketil Heimdal, et al.
Laryngoscope Investigative Otolaryngology|February 16, 2024
Elevated FVIII levels in hereditary hemorrhagic telangiectasia: Implications for clinical managementOle Jakob Jørgensen, Johan Edvard Steineger, Andreas Hillarp, et al.
International Journal of Audiology|June 18, 2010
Causes of hearing impairment in the Norwegian paediatric cochlear implant programGeir Siem, Toril Fagerheim, Christoffer Jonsrud, et al.
Disease Markers|March 1, 2005
Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from NorwayPetter Frost, Astanand Jugessur, Jaran Apold, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 22, 2005
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancerAstrid T Stormorken, Inger Marie Bowitz-Lothe, Tove Norèn, et al.
Cancers|April 30, 2021
Histological Features of Sporadic and Familial Testicular Germ Cell Tumors Compared and Analysis of Age-Related Changes of HistologyAndreas Stang, Mary L McMaster, Isabell A Sesterhenn, et al.
Familial Cancer|October 24, 2003
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumoursAstrid T Stormorken, Wolfram Müller, Annika Lindblom, et al.
Public Health Genomics|September 18, 2014
National registries of rare diseases in Europe: an overview of the current situation and experiencesDomenica Taruscio, Luciano Vittozzi, Remy Choquet, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Pediatric Pulmonology|September 18, 2024
Tracheobronchomalacia is common in children with primary ciliary dyskinesia-A case note reviewSynne S Kennelly, Vegard Hovland, Iren Lindbak Matthews, et al.
Plos One|July 9, 2015
A Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1Irene Johnsrud, Mari Ann Kulseth, Olaug Kristin Rødningen, et al.
Acta Oto-Laryngologica|December 15, 2020
Head and neck paragangliomas in Norway, importance of genetics, updated diagnostic workup and treatmentMohammad Usman Rana, Arild André Østhus, Ketil Heimdal, et al.
Laryngoscope Investigative Otolaryngology|February 16, 2024
Elevated FVIII levels in hereditary hemorrhagic telangiectasia: Implications for clinical managementOle Jakob Jørgensen, Johan Edvard Steineger, Andreas Hillarp, et al.
International Journal of Audiology|June 18, 2010
Causes of hearing impairment in the Norwegian paediatric cochlear implant programGeir Siem, Toril Fagerheim, Christoffer Jonsrud, et al.
Disease Markers|March 1, 2005
Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from NorwayPetter Frost, Astanand Jugessur, Jaran Apold, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 22, 2005
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancerAstrid T Stormorken, Inger Marie Bowitz-Lothe, Tove Norèn, et al.
Cancers|April 30, 2021
Histological Features of Sporadic and Familial Testicular Germ Cell Tumors Compared and Analysis of Age-Related Changes of HistologyAndreas Stang, Mary L McMaster, Isabell A Sesterhenn, et al.
Familial Cancer|October 24, 2003
The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumoursAstrid T Stormorken, Wolfram Müller, Annika Lindblom, et al.
Public Health Genomics|September 18, 2014
National registries of rare diseases in Europe: an overview of the current situation and experiencesDomenica Taruscio, Luciano Vittozzi, Remy Choquet, et al.
Pageof 6