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Leena Valanne

Showing results (61-70 of 70) with videos related to

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European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|October 11, 2020
Predictive Factors for Pre-operative Recurrence of Cerebrovascular Symptoms in Symptomatic Carotid StenosisHenrietta Eriksson, Suvi Koskinen, Krista Nuotio, et al.
The American Journal of Psychiatry|August 31, 2002
Contributions of genetic risk and fetal hypoxia to hippocampal volume in patients with schizophrenia or schizoaffective disorder, their unaffected siblings, and healthy unrelated volunteersTheo G M Van Erp, Peter A Saleh, Isabelle M Rosso, et al.
Human Molecular Genetics|July 27, 2012
Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathyJenni M Elo, Srujana S Yadavalli, Liliya Euro, et al.
Annals of Medicine|July 17, 2018
Morphology and histology of silent and symptom-causing atherosclerotic carotid plaques - Rationale and design of the Helsinki Carotid Endarterectomy Study 2 (the HeCES2)Krista Nuotio, Petra Ijäs, Hanna M Heikkilä, et al.
Pediatric Blood & Cancer|April 3, 2014
Radiation therapy and concurrent topotecan followed by maintenance triple anti-angiogenic therapy with thalidomide, etoposide, and celecoxib for pediatric diffuse intrinsic pontine gliomaMikaela Porkholm, Leena Valanne, Tuula Lönnqvist, et al.
Frontiers in Neurology|July 29, 2021
Warfarin Treatment Is Associated to Increased Internal Carotid Artery CalcificationKrista Nuotio, Suvi M Koskinen, Laura Mäkitie, et al.
Neurology|June 28, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactateAnna-Kaisa Anttonen, Taru Hilander, Tarja Linnankivi, et al.
Brain : a Journal of Neurology|March 24, 2017
ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron lossAnna-Kaisa Anttonen, Anni Laari, Maria Kousi, et al.
JAMA|March 16, 2016
Effect of Inhaled Xenon on Cerebral White Matter Damage in Comatose Survivors of Out-of-Hospital Cardiac Arrest: A Randomized Clinical TrialRuut Laitio, Marja Hynninen, Olli Arola, et al.
Nature Communications|November 4, 2017
Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosisJohanna Tommiska, Johanna Känsäkoski, Lasse Skibsbye, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|October 11, 2020
Predictive Factors for Pre-operative Recurrence of Cerebrovascular Symptoms in Symptomatic Carotid StenosisHenrietta Eriksson, Suvi Koskinen, Krista Nuotio, et al.
The American Journal of Psychiatry|August 31, 2002
Contributions of genetic risk and fetal hypoxia to hippocampal volume in patients with schizophrenia or schizoaffective disorder, their unaffected siblings, and healthy unrelated volunteersTheo G M Van Erp, Peter A Saleh, Isabelle M Rosso, et al.
Human Molecular Genetics|July 27, 2012
Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathyJenni M Elo, Srujana S Yadavalli, Liliya Euro, et al.
Annals of Medicine|July 17, 2018
Morphology and histology of silent and symptom-causing atherosclerotic carotid plaques - Rationale and design of the Helsinki Carotid Endarterectomy Study 2 (the HeCES2)Krista Nuotio, Petra Ijäs, Hanna M Heikkilä, et al.
Pediatric Blood & Cancer|April 3, 2014
Radiation therapy and concurrent topotecan followed by maintenance triple anti-angiogenic therapy with thalidomide, etoposide, and celecoxib for pediatric diffuse intrinsic pontine gliomaMikaela Porkholm, Leena Valanne, Tuula Lönnqvist, et al.
Frontiers in Neurology|July 29, 2021
Warfarin Treatment Is Associated to Increased Internal Carotid Artery CalcificationKrista Nuotio, Suvi M Koskinen, Laura Mäkitie, et al.
Neurology|June 28, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactateAnna-Kaisa Anttonen, Taru Hilander, Tarja Linnankivi, et al.
Brain : a Journal of Neurology|March 24, 2017
ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron lossAnna-Kaisa Anttonen, Anni Laari, Maria Kousi, et al.
JAMA|March 16, 2016
Effect of Inhaled Xenon on Cerebral White Matter Damage in Comatose Survivors of Out-of-Hospital Cardiac Arrest: A Randomized Clinical TrialRuut Laitio, Marja Hynninen, Olli Arola, et al.
Nature Communications|November 4, 2017
Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosisJohanna Tommiska, Johanna Känsäkoski, Lasse Skibsbye, et al.
Pageof 7