Obara-Moszyńska, Monika: search on Z-Library

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1

A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment

Monika Obara-Moszynska, Jaroslaw Maceluch, Waldemar Bobkowski…

Journal:

Year:

2013

Language:

english

File:

PDF, 597 KB

english, 2013

2

NR0B1(DAX1) mutations in patients affected by congenital adrenal hypoplasia with growth hormone deficiency as a new finding

Aleksandra Rojek, Monika Obara-Moszynska, Elzbieta Malecka…

Journal:

Journal of Applied Genetics

Year:

2013

Language:

english

File:

PDF, 206 KB

english, 2013

3

Treatment of cartilage-hair hypoplasia with recombinant human growth hormone

Obara-Moszynska, Monika, Wielanowska, Weronika, Rojek, Aleksandra, Wolnik-Brzozowska, Danuta, Niedziela, Marek

Journal:

Pediatrics International

Year:

2013

Language:

english

File:

PDF, 337 KB

english, 2013

4

Exome sequencing reveals two novel compound heterozygous XYLT1 mutations in a Polish patient with Desbuquois dysplasia type 2 and growth hormone deficiency

Jamsheer, Aleksander, Olech, Ewelina M, Kozłowski, Kazimierz, Niedziela, Marek, Sowińska-Seidler, Anna, Obara-Moszyńska, Monika, Latos-Bieleńska, Anna, Karczewski, Marek, Zemojtel, Tomasz

Journal:

Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.44 MB

english, 2016

5

Pituitary Microsomal Autoantibodies in Patients with Childhood-Onset Combined Pituitary Hormone Deficiency: an Antigen Identification Attempt

Ziemnicka, Katarzyna, Gut, Paweł, Gołąb, Monika, Dworacki, Grzegorz, Wrotkowska, Elżbieta, Stajgis, Marek, Katulska, Katarzyna, Rabska-Pietrzak, Barbara, Obara-Moszyńska, Monika, Niedziela, Marek, Bud

Journal:

Archivum Immunologiae et Therapiae Experimentalis

Year:

2016

Language:

english

File:

PDF, 1.06 MB

english, 2016

6

Bridging clinical care and basic research

Niedziela, Marek, Rojek, Aleksandra, Obara-Moszynska, Monika

Journal:

Pediatric Health

Year:

2010

Language:

english

File:

PDF, 361 KB

english, 2010

7

Idiopathic short stature, current knowledge and perspectives – Review article

Rohde, Anna, Obara-Moszynska, Monika

Journal:

Pediatria Polska

Year:

2017

Language:

english

File:

PDF, 319 KB

english, 2017

8

Molecular Detection and Incidence of Y Chromosomal Material in Patients with Turner Syndrome

Rojek, Aleksandra, Obara-Moszynska, Monika, Kolesinska, Zofia, Rabska-Pietrzak, Barbara, Niedziela, Marek

Journal:

Sexual Development

Year:

2017

Language:

english

File:

PDF, 140 KB

english, 2017

9

Diabetes insipidus coexisting with sellar-suprasellar tumor –

Obara-Moszyńska, Monika, Perek, Danuta, Mikoś, Hanna, Niedziela, Marek

Journal:

Współczesna Onkologia

Year:

2011

Language:

english

File:

PDF, 448 KB

english, 2011

10

The Usefulness of Magnetic Resonance Imaging of the Cardiovascular System in the Diagnostic Work-Up of Patients With Turner Syndrome

Obara-Moszynska, Monika, Rajewska-Tabor, Justyna, Rozmiarek, Szymon, Karmelita-Katulska, Katarzyna, Kociemba, Anna, Rabska-Pietrzak, Barbara, Janus, Magdalena, Siniawski, Andrzej, Mrozinski, Bartlomie

Journal:

Frontiers in Endocrinology

Year:

2018

Language:

english

File:

PDF, 1.46 MB

english, 2018

11

SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD)

Budny, Bartlomiej, Zemojtel, Tomasz, Kaluzna, Malgorzata, Gut, Pawel, Niedziela, Marek, Obara-Moszynska, Monika, Rabska-Pietrzak, Barbara, Karmelita-Katulska, Katarzyna, Stajgis, Marek, Ambroziak, Urs

Journal:

Frontiers in Endocrinology

Year:

2020

File:

PDF, 791 KB

2020