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Martin Lammens

Showing results (31-40 of 91) with videos related to

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Arthritis Research & Therapy|June 3, 2014
Scleroderma-polymyositis overlap syndrome versus idiopathic polymyositis and systemic sclerosis: a descriptive study on clinical features and myopathologyKavish J Bhansing, Martin Lammens, Hanneke K A Knaapen, et al.
European Journal of Pediatrics|November 2, 2004
Brain-Thyroid-Lung syndrome: a patient with a severe multi-system disorder due to a de novo mutation in the thyroid transcription factor 1 geneMichel A A P Willemsen, Guido J Breedveld, Siep Wouda, et al.
Surgical Neurology International|February 2, 2013
Correlation between contrast enhancement on intraoperative magnetic resonance imaging and histopathology in glioblastomaPieter L Kubben, Pieter Wesseling, Martin Lammens, et al.
Neuromuscular Disorders : NMD|December 16, 2014
A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmyBeverly Jo McCann, Helen A L Tuppen, Benno Küsters, et al.
Journal of Neuropathology and Experimental Neurology|September 26, 2019
Neuroinflammation and Not Tauopathy Is a Predominant Pathological Signature of Nodding SyndromeAn Hotterbeekx, Martin Lammens, Richard Idro, et al.
Cancer Immunology, Immunotherapy : CII|September 13, 2019
Desmoid tumors display a strong immune infiltration at the tumor margins and no PD-L1-driven immune suppressionVasiliki Siozopoulou, Elly Marcq, Julie Jacobs, et al.
Clinical Genetics|April 26, 2020
Expanding the clinical spectrum of Fowler syndrome: Three siblings with survival into adulthood and systematic review of the literatureChiara De Luca, Yanick J Crow, Mathieu Rodero, et al.
Plos One|November 11, 2020
The clinical value of minimal invasive autopsy in COVID-19 patientsValentino D'Onofrio, Elena Donders, Marie-Elena Vanden Abeele, et al.
The Journal of Cell Biology|January 18, 2007
Nucleoplasmic LAP2alpha-lamin A complexes are required to maintain a proliferative state in human fibroblastsVanja Pekovic, Jens Harborth, Jos L V Broers, et al.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
Pageof 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
Arthritis Research & Therapy|June 3, 2014
Scleroderma-polymyositis overlap syndrome versus idiopathic polymyositis and systemic sclerosis: a descriptive study on clinical features and myopathologyKavish J Bhansing, Martin Lammens, Hanneke K A Knaapen, et al.
European Journal of Pediatrics|November 2, 2004
Brain-Thyroid-Lung syndrome: a patient with a severe multi-system disorder due to a de novo mutation in the thyroid transcription factor 1 geneMichel A A P Willemsen, Guido J Breedveld, Siep Wouda, et al.
Surgical Neurology International|February 2, 2013
Correlation between contrast enhancement on intraoperative magnetic resonance imaging and histopathology in glioblastomaPieter L Kubben, Pieter Wesseling, Martin Lammens, et al.
Neuromuscular Disorders : NMD|December 16, 2014
A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmyBeverly Jo McCann, Helen A L Tuppen, Benno Küsters, et al.
Journal of Neuropathology and Experimental Neurology|September 26, 2019
Neuroinflammation and Not Tauopathy Is a Predominant Pathological Signature of Nodding SyndromeAn Hotterbeekx, Martin Lammens, Richard Idro, et al.
Cancer Immunology, Immunotherapy : CII|September 13, 2019
Desmoid tumors display a strong immune infiltration at the tumor margins and no PD-L1-driven immune suppressionVasiliki Siozopoulou, Elly Marcq, Julie Jacobs, et al.
Clinical Genetics|April 26, 2020
Expanding the clinical spectrum of Fowler syndrome: Three siblings with survival into adulthood and systematic review of the literatureChiara De Luca, Yanick J Crow, Mathieu Rodero, et al.
Plos One|November 11, 2020
The clinical value of minimal invasive autopsy in COVID-19 patientsValentino D'Onofrio, Elena Donders, Marie-Elena Vanden Abeele, et al.
The Journal of Cell Biology|January 18, 2007
Nucleoplasmic LAP2alpha-lamin A complexes are required to maintain a proliferative state in human fibroblastsVanja Pekovic, Jens Harborth, Jos L V Broers, et al.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
Pageof 10