M. Obara-Moszyńska

发表

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

A. Rojek, M. Niedziela, Z. Kolesinska, 2017, Sexual Development.

Growth hormone treatment in pituitary insufficiency: selected cases of children with craniopharyngioma and medulloblastoma.

P. Kopinski, J. Trojan, A. Gozdzicka-Jozefiak, 2003, Roczniki Akademii Medycznej w Bialymstoku.

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

M. Pyda, M. Niedziela, K. Karmelita-Katulska, 2018, Front. Endocrinol..

The influence of growth hormone therapy on the cardiovascular system in Turner syndrome

M. Niedziela, M. Obara-Moszyńska, Kamil Dyrka, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

The role of the immune system and cytokines involved in the pathogenesis of autoimmune thyroid disease (AITD) Rola układu immunologicznego oraz udział cytokin w patomechanizmie autoimmunologicznej choroby tarczycy (AITD)

M. Niedziela, M. Obara-Moszyńska, M. Niedziela, 2014 .

Assessment of ghrelin, GHS-R, GH, and neurohormones in human fetal pituitary glands and central nervous system: an immunohistochemical study.

Maria Chmielnicka-Kopaczyk, M. Obara-Moszyńska, A. Kędzia, 2010, Folia histochemica et cytobiologica.

X-linked hypophosphatemic rickets in children: clinical phenotype, therapeutic strategies and molecular background.

K. Chrzanowska, A. Rojek, M. Niedziela, 2020, Endokrynologia Polska.

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

M. Krawczyński, M. Niedziela, W. Bobkowski, 2013, BMC Pediatrics.

The usefulness of the GHRH stimulation test in the diagnostics of growth hormone deficiency in children.

M. Niedziela, M. Obara-Moszyńska, 2015, Endokrynologia Polska.

Effects of Recombinant Human Growth Hormone Treatment, Depending on the Therapy Start in Different Nutritional Phases in Paediatric Patients with Prader–Willi Syndrome: A Polish Multicentre Study

M. Szalecki, E. Petriczko, A. Zygmunt-Górska, 2021, Journal of clinical medicine.

Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Prader–Willi Syndrome

M. Szalecki, E. Petriczko, A. Zygmunt-Górska, 2021, Diagnostics.

Case report: The cardio-facio-cutaneous syndrome due to a novel germline mutation in MAP2K1: A multifaceted disease with immunodeficiency and short stature

M. Niedziela, P. Sztromwasser, A. Szczawinska-Poplonyk, 2022, Frontiers in Pediatrics.

The role of the immune system and cytokines involved in the pathogenesis of autoimmune thyroid disease (AITD).

M. Niedziela, M. Mikoś, M. Obara-Moszyńska, 2014, Endokrynologia Polska.

Idiopathic short stature, current knowledge and perspectives – Review article

M. Obara-Moszyńska, A. Rohde, 2017 .

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

T. Żemojtel, P. Gut, M. Ruchała, 2020, Frontiers in Endocrinology.

Growth hormone therapy in a girl with Turner syndrome and diabetes type 1 - case report.

M. Niedziela, M. Obara-Moszyńska, M. Banaszak, 2014, Pediatric endocrinology, diabetes, and metabolism.

Growth hormone therapy in a girl with Turner syndrome and diabetes type 1 - case report Leczenie rekombinowanym hormonem wzrostu dziewczynki z zespołem Turnera i cukrzycą typu 1 - opis przypadku

M. Niedziela, M. Obara-Moszyńska, M. Banaszak, 2015 .

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

P. Gut, M. Ruchała, M. Niedziela, 2016, Archivum Immunologiae et Therapiae Experimentalis.

Treatment of cartilage–hair hypoplasia with recombinant human growth hormone

A. Rojek, M. Niedziela, M. Obara-Moszyńska, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

CDON gene contributes to pituitary stalk interruption syndrome associated with unilateral facial and abducens nerve palsy

M. Ruchała, M. Niedziela, K. Zawadzka, 2021, Journal of Applied Genetics.

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

A. Rojek, M. Niedziela, E. Małecka, 2013, Journal of Applied Genetics.

Usefulness of Growth Hormone (GH) Stimulation Tests and IGF-1 Concentration Measurement in GH Deficiency Diagnosis

M. Niedziela, M. Obara-Moszyńska, E. Korman, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Uterine Development During Induced Puberty in Girls with Turner Syndrome

M. Niedziela, M. Obara-Moszyńska, B. Rabska-Pietrzak, 2021, Frontiers in Endocrinology.

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

A. Latos-Bieleńska, T. Żemojtel, M. Niedziela, 2016, Journal of Human Genetics.

The effects of growth hormone treatment in patients with somatotropin deficiency during their developmental age.

M. Obara-Moszyńska, B. Rabska-Pietrzak, A. Kędzia, 2005, Endokrynologia Polska.

Expression of ghrelin in human fetal adrenal glands and paraadrenal nerve ganglions.

Maria Chmielnicka-Kopaczyk, M. Obara-Moszyńska, A. Kędzia, 2009, Folia histochemica et cytobiologica.