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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

artículo científico publicado en 2013

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

artículo científico publicado en 2009

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

artículo científico publicado en 2021

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

artículo científico publicado en 2016

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

artículo científico publicado en 2009

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

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

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

artículo científico publicado en 2016

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

artículo científico publicado en 2020

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

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

artículo científico publicado en 2005

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

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Treatment of cartilage-hair hypoplasia with recombinant human growth hormone.

artículo científico publicado en 2013

Usefulness of growth hormone (GH) stimulation tests and IGF-I concentration measurement in GH deficiency diagnosis

artículo científico publicado en 2008

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

scientific article published on 09 December 2020

Y chromosome in Turner syndrome

artículo científico publicado en 2017

[Estimation of growth hormone secretion during sleep as a screening test in the diagnosis of GH deficiency]

artículo científico publicado en 2006

[High level of hsCRP in patients with Graves' ophthalmopathy--preliminary study]

artículo científico publicado en 2004

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