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Marjo Kestilä

Showing results (1-10 of 29) with videos related to

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Prenatal Diagnosis|April 4, 2003
Prenatal diagnosis of congenital nephrotic syndrome (CNF, NPHS1)Marjo Kestilä, Irma Järvelä
Duodecim; Laaketieteellinen Aikakauskirja|November 20, 2010
[Finnish disease heritage]Marjo Kestilä, Elina Ikonen, Anna-Elina Lehesjoki
Clinical and Experimental Nephrology|August 14, 2014
Podocyte proteins in congenital and minimal change nephrotic syndromeMaija Suvanto, Timo Jahnukainen, Marjo Kestilä, et al.
International Journal of Nephrology|June 2, 2016
Single Nucleotide Polymorphisms in Pediatric Idiopathic Nephrotic SyndromeMaija Suvanto, Timo Jahnukainen, Marjo Kestilä, et al.
Human Mutation|May 26, 2009
Mutation spectrum of Meckel syndrome genes: one group of syndromes or several distinct groups?Jonna Tallila, Riitta Salonen, Nicolai Kohlschmidt, et al.
American Journal of Human Genetics|June 3, 2008
Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzleJonna Tallila, Eveliina Jakkula, Leena Peltonen, et al.
Kidney International|April 17, 2004
Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS)Anne-Tiina Lahdenkari, Marjo Kestilä, Christer Holmberg, et al.
Archives of Dermatology|May 18, 2005
A patient with Rothmund-Thomson syndrome and all features of RAPADILINORichard Kellermayer, H Annika Siitonen, Kinga Hadzsiev, et al.
Journal of Neuropathology and Experimental Neurology|July 24, 2008
Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysisAnders Paetau, Heli Honkala, Riitta Salonen, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
Lethal congenital contracture syndrome (LCCS) and other lethal arthrogryposes in Finland--an epidemiological studyNiklas Pakkasjärvi, Annukka Ritvanen, Riitta Herva, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|April 4, 2003
Prenatal diagnosis of congenital nephrotic syndrome (CNF, NPHS1)Marjo Kestilä, Irma Järvelä
Duodecim; Laaketieteellinen Aikakauskirja|November 20, 2010
[Finnish disease heritage]Marjo Kestilä, Elina Ikonen, Anna-Elina Lehesjoki
Clinical and Experimental Nephrology|August 14, 2014
Podocyte proteins in congenital and minimal change nephrotic syndromeMaija Suvanto, Timo Jahnukainen, Marjo Kestilä, et al.
International Journal of Nephrology|June 2, 2016
Single Nucleotide Polymorphisms in Pediatric Idiopathic Nephrotic SyndromeMaija Suvanto, Timo Jahnukainen, Marjo Kestilä, et al.
Human Mutation|May 26, 2009
Mutation spectrum of Meckel syndrome genes: one group of syndromes or several distinct groups?Jonna Tallila, Riitta Salonen, Nicolai Kohlschmidt, et al.
American Journal of Human Genetics|June 3, 2008
Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzleJonna Tallila, Eveliina Jakkula, Leena Peltonen, et al.
Kidney International|April 17, 2004
Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS)Anne-Tiina Lahdenkari, Marjo Kestilä, Christer Holmberg, et al.
Archives of Dermatology|May 18, 2005
A patient with Rothmund-Thomson syndrome and all features of RAPADILINORichard Kellermayer, H Annika Siitonen, Kinga Hadzsiev, et al.
Journal of Neuropathology and Experimental Neurology|July 24, 2008
Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysisAnders Paetau, Heli Honkala, Riitta Salonen, et al.
American Journal of Medical Genetics. Part A|August 8, 2006
Lethal congenital contracture syndrome (LCCS) and other lethal arthrogryposes in Finland--an epidemiological studyNiklas Pakkasjärvi, Annukka Ritvanen, Riitta Herva, et al.
Pageof 3