D Jurkiewicz - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

D Jurkiewicz

Showing results (41-50 of 46) with videos related to

Pageof 5

Sort By:

You have reached the last page of results.This site can display upto 46 results.

Journal of Applied Genetics|October 18, 2003

X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX geneE Popowska, E Pronicka, A Sułek, et al.

Polski Tygodnik Lekarski (Warsaw, Poland : 1960)|July 16, 1990

[Three month treatment with budesonide in patients with corticoid dependent bronchial asthma--personal experience]A Frank-Piskorska, Z Wasek, K Jahnz-Rózyk, et al.

Journal of Applied Genetics|October 18, 2003

X-linked hypophosphatemia in Polish patients. 2. Analysis of clinical features and genotype-phenotype correlationE Popowska, E Pronicka, A Sułek, et al.

Clinical Genetics|March 19, 2013

RSK2 mutation co-segregates with X-linked intellectual disability and attenuated Coffin-Lowry phenotype in a three-generation familyI Maystadt, A Destree, V Benoit, et al.

European Journal of Medical Genetics|February 25, 2006

SLOS carrier frequency in Poland as determined by screening for Trp151X and Val326Leu DHCR7 mutationsE Ciara, E Popowska, D Piekutowska-Abramczuk, et al.

Clinical Genetics|July 9, 2013

Novel c.191C>G (p.Pro64Arg) MPV17 mutation identified in two pairs of unrelated Polish siblings with mitochondrial hepatoencephalopathyD Piekutowska-Abramczuk, M Pronicki, K Strawa, et al.

Pageof 5

Search research articles

Showing results (41-50 of 46) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 46 results.

Journal of Applied Genetics|October 18, 2003

X-linked hypophosphatemia in Polish patients. 1. Mutations in the PHEX geneE Popowska, E Pronicka, A Sułek, et al.

Polski Tygodnik Lekarski (Warsaw, Poland : 1960)|July 16, 1990

[Three month treatment with budesonide in patients with corticoid dependent bronchial asthma--personal experience]A Frank-Piskorska, Z Wasek, K Jahnz-Rózyk, et al.

Journal of Applied Genetics|October 18, 2003

X-linked hypophosphatemia in Polish patients. 2. Analysis of clinical features and genotype-phenotype correlationE Popowska, E Pronicka, A Sułek, et al.

Clinical Genetics|March 19, 2013

RSK2 mutation co-segregates with X-linked intellectual disability and attenuated Coffin-Lowry phenotype in a three-generation familyI Maystadt, A Destree, V Benoit, et al.

European Journal of Medical Genetics|February 25, 2006

SLOS carrier frequency in Poland as determined by screening for Trp151X and Val326Leu DHCR7 mutationsE Ciara, E Popowska, D Piekutowska-Abramczuk, et al.

Clinical Genetics|July 9, 2013

Novel c.191C>G (p.Pro64Arg) MPV17 mutation identified in two pairs of unrelated Polish siblings with mitochondrial hepatoencephalopathyD Piekutowska-Abramczuk, M Pronicki, K Strawa, et al.

Pageof 5