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Anna-Kaisa Niemi

Showing results (1-10 of 31) with videos related to

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Children (Basel, Switzerland)|April 4, 2017
Review of Randomized Controlled Trials of Massage in Preterm InfantsAnna-Kaisa Niemi
Neoreviews|October 2, 2020
Neonatal Presentations of Metabolic DisordersAnna-Kaisa Niemi Md
European Journal of Human Genetics : EJHG|May 12, 2005
Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletesAnna-Kaisa Niemi, Kari Majamaa
Platelets|December 14, 2021
Severe thrombocytopenia and intracranial hemorrhage in a newborn with Noonan syndrome and neonatal alloimmune thrombocytopeniaRebecca Carter, Anna-Kaisa Niemi
The Journal of Pediatrics|March 12, 2019
Near-Infrared Spectroscopy in the Diagnostic Evaluation of Mitochondrial Disorders: A Neonatal Intensive Care Unit Case SeriesAnna-Kaisa Niemi, Valerie Y Chock
The Journal of Pediatrics|September 13, 2015
Reply: To PMID 25771389Anna-Kaisa Niemi, Gregory M Enns
American Journal of Medical Genetics. Part A|September 13, 2011
Horseshoe kidney and a rare TSC2 variant in two unrelated individuals with tuberous sclerosis complexAnna-Kaisa Niemi, Hope Northrup, Louanne Hudgins, et al.
Ultrastructural Pathology|June 17, 2014
Abnormal hepatocellular mitochondria in methylmalonic acidemiaYael Wilnai, Gregory M Enns, Anna-Kaisa Niemi, et al.
BMC Genomics|October 31, 2019
Analysis of functional variants in mitochondrial DNA of Finnish athletesJukka Kiiskilä, Jukka S Moilanen, Laura Kytövuori, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Report of two patients and further characterization of interstitial 9p13 deletion--a rare but recurrent microdeletion syndrome?Anna-Kaisa Niemi, Andrea Kwan, Louanne Hudgins, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Children (Basel, Switzerland)|April 4, 2017
Review of Randomized Controlled Trials of Massage in Preterm InfantsAnna-Kaisa Niemi
Neoreviews|October 2, 2020
Neonatal Presentations of Metabolic DisordersAnna-Kaisa Niemi Md
European Journal of Human Genetics : EJHG|May 12, 2005
Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletesAnna-Kaisa Niemi, Kari Majamaa
Platelets|December 14, 2021
Severe thrombocytopenia and intracranial hemorrhage in a newborn with Noonan syndrome and neonatal alloimmune thrombocytopeniaRebecca Carter, Anna-Kaisa Niemi
The Journal of Pediatrics|March 12, 2019
Near-Infrared Spectroscopy in the Diagnostic Evaluation of Mitochondrial Disorders: A Neonatal Intensive Care Unit Case SeriesAnna-Kaisa Niemi, Valerie Y Chock
The Journal of Pediatrics|September 13, 2015
Reply: To PMID 25771389Anna-Kaisa Niemi, Gregory M Enns
American Journal of Medical Genetics. Part A|September 13, 2011
Horseshoe kidney and a rare TSC2 variant in two unrelated individuals with tuberous sclerosis complexAnna-Kaisa Niemi, Hope Northrup, Louanne Hudgins, et al.
Ultrastructural Pathology|June 17, 2014
Abnormal hepatocellular mitochondria in methylmalonic acidemiaYael Wilnai, Gregory M Enns, Anna-Kaisa Niemi, et al.
BMC Genomics|October 31, 2019
Analysis of functional variants in mitochondrial DNA of Finnish athletesJukka Kiiskilä, Jukka S Moilanen, Laura Kytövuori, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Report of two patients and further characterization of interstitial 9p13 deletion--a rare but recurrent microdeletion syndrome?Anna-Kaisa Niemi, Andrea Kwan, Louanne Hudgins, et al.
Pageof 4