Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Timo Jahnukainen

Showing results (81-90 of 122) with videos related to

Pageof 13
Sort By:
Scientific Reports|July 6, 2016
COL4A6 is dispensable for autosomal recessive Alport syndromeTomohiro Murata, Kan Katayama, Toshitaka Oohashi, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|February 27, 2022
Liver pathology and biochemistry in patients with mutations in TRIM37 gene (Mulibrey nanism)Johanna Sivunen, Susann Karlberg, Reetta Kivisaari, et al.
Archives of Disease in Childhood|April 8, 2010
Clinical course of extrarenal symptoms in Henoch-Schonlein purpura: a 6-month prospective studyOuti Jauhola, Jaana Ronkainen, Olli Koskimies, et al.
Pediatric Nephrology (Berlin, Germany)|February 8, 2012
Outcome of Henoch-Schönlein purpura 8 years after treatment with a placebo or prednisone at disease onsetOuti Jauhola, Jaana Ronkainen, Olli Koskimies, et al.
Pediatric Nephrology (Berlin, Germany)|February 16, 2017
The ISKDC classification and a new semiquantitative classification for predicting outcomes of Henoch-Schönlein purpura nephritisMikael Koskela, Elisa Ylinen, Elli-Maija Ukonmaanaho, et al.
The Journal of Infectious Diseases|May 20, 2024
Reactivation of a Transplant Recipient's Inherited Human Herpesvirus 6 and Implications to the GraftLeo Hannolainen, Lari Pyöriä, Diogo Pratas, et al.
Pediatric Nephrology (Berlin, Germany)|July 14, 2006
Long-term outcome 19 years after childhood IgA nephritis: a retrospective cohort studyJaana Ronkainen, Marja Ala-Houhala, Helena Autio-Harmainen, et al.
Scientific Reports|November 19, 2020
Inactivation of mediator complex protein 22 in podocytes results in intracellular vacuole formation, podocyte loss and premature deathPatricia Q Rodriguez, David Unnersjö-Jess, Sonia S Zambrano, et al.
Transplantation Direct|September 25, 2023
Recurrent Mild Acute Rejections and Donor-specific Antibodies as Risk Factors for Cardiac Allograft Vasculopathy in a National Pediatric Heart Transplant CohortAnu K Kaskinen, Juuso Tainio, Jaana I Pihkala, et al.
Archives of Disease in Childhood|September 21, 2010
Renal manifestations of Henoch-Schonlein purpura in a 6-month prospective study of 223 childrenOuti Jauhola, Jaana Ronkainen, Olli Koskimies, et al.
Pageof 13

Showing results (81-90 of 122) with videos related to

Sort By:
Pageof 13
Scientific Reports|July 6, 2016
COL4A6 is dispensable for autosomal recessive Alport syndromeTomohiro Murata, Kan Katayama, Toshitaka Oohashi, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|February 27, 2022
Liver pathology and biochemistry in patients with mutations in TRIM37 gene (Mulibrey nanism)Johanna Sivunen, Susann Karlberg, Reetta Kivisaari, et al.
Archives of Disease in Childhood|April 8, 2010
Clinical course of extrarenal symptoms in Henoch-Schonlein purpura: a 6-month prospective studyOuti Jauhola, Jaana Ronkainen, Olli Koskimies, et al.
Pediatric Nephrology (Berlin, Germany)|February 8, 2012
Outcome of Henoch-Schönlein purpura 8 years after treatment with a placebo or prednisone at disease onsetOuti Jauhola, Jaana Ronkainen, Olli Koskimies, et al.
Pediatric Nephrology (Berlin, Germany)|February 16, 2017
The ISKDC classification and a new semiquantitative classification for predicting outcomes of Henoch-Schönlein purpura nephritisMikael Koskela, Elisa Ylinen, Elli-Maija Ukonmaanaho, et al.
The Journal of Infectious Diseases|May 20, 2024
Reactivation of a Transplant Recipient's Inherited Human Herpesvirus 6 and Implications to the GraftLeo Hannolainen, Lari Pyöriä, Diogo Pratas, et al.
Pediatric Nephrology (Berlin, Germany)|July 14, 2006
Long-term outcome 19 years after childhood IgA nephritis: a retrospective cohort studyJaana Ronkainen, Marja Ala-Houhala, Helena Autio-Harmainen, et al.
Scientific Reports|November 19, 2020
Inactivation of mediator complex protein 22 in podocytes results in intracellular vacuole formation, podocyte loss and premature deathPatricia Q Rodriguez, David Unnersjö-Jess, Sonia S Zambrano, et al.
Transplantation Direct|September 25, 2023
Recurrent Mild Acute Rejections and Donor-specific Antibodies as Risk Factors for Cardiac Allograft Vasculopathy in a National Pediatric Heart Transplant CohortAnu K Kaskinen, Juuso Tainio, Jaana I Pihkala, et al.
Archives of Disease in Childhood|September 21, 2010
Renal manifestations of Henoch-Schonlein purpura in a 6-month prospective study of 223 childrenOuti Jauhola, Jaana Ronkainen, Olli Koskimies, et al.
Pageof 13