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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 Stenosis
Henrietta 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 volunteers
Theo 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 encephalopathy
Jenni 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 glioma
Mikaela Porkholm, Leena Valanne, Tuula Lönnqvist, et al.
Frontiers in Neurology
|
July 29, 2021
Warfarin Treatment Is Associated to Increased Internal Carotid Artery Calcification
Krista Nuotio, Suvi M Koskinen, Laura Mäkitie, et al.
Neurology
|
June 28, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate
Anna-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 loss
Anna-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 Trial
Ruut 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 fibromatosis
Johanna Tommiska, Johanna Känsäkoski, Lasse Skibsbye, et al.
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Search research articles
Search
Showing results (61-70 of 70) with videos related to
Sort By:
Page
of 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 Stenosis
Henrietta 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 volunteers
Theo 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 encephalopathy
Jenni 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 glioma
Mikaela Porkholm, Leena Valanne, Tuula Lönnqvist, et al.
Frontiers in Neurology
|
July 29, 2021
Warfarin Treatment Is Associated to Increased Internal Carotid Artery Calcification
Krista Nuotio, Suvi M Koskinen, Laura Mäkitie, et al.
Neurology
|
June 28, 2015
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate
Anna-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 loss
Anna-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 Trial
Ruut 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 fibromatosis
Johanna Tommiska, Johanna Känsäkoski, Lasse Skibsbye, et al.
Page
of 7