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Autoimmune thyroiditis: an update on treatment possibilities.
- Published in:
- Polish Journal of Endocrinology / Endokrynologia Polska, 2024, v. 75, n. 5, p. 461, doi. 10.5603/ep.100701
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- Article
Syndrome of Congenital Insulin Resistance Caused by a Novel INSR Gene Mutation.
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- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 3, p. 312, doi. 10.4274/jcrpe.galenos.2021.2021.0256
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- Article
Moderate congenital adrenal hyperplasia in two girls diagnosed by newborn screening.
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- Pediatric Endocrinology, Diabetes & Metabolism, 2021, v. 27, n. 4, p. 291, doi. 10.5114/pedm.2021.109123
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- Article
Is growth without IGF1 possible? A case report.
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- Pediatric Endocrinology, Diabetes & Metabolism, 2017, v. 23, n. 4, p. 215, doi. 10.18544/PEDM-23.04.0096
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- Article
Chromosom Y w zespole Turnera.
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- Pediatric Endocrinology, Diabetes & Metabolism, 2017, v. 23, n. 1, p. 37, doi. 10.18544/PEDM-23.01.0072
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- Article
Growth hormone therapy in a girl with Turner syndrome and diabetes type 1 - case report.
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- Pediatric Endocrinology, Diabetes & Metabolism, 2014, v. 20, n. 2, p. 75
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- Article
Analiza ekspresji wewnątrzkomórkowych proapoptotycznych (Box, Bak) i antyapoptotycznych (Bcl-2, Bcl-XL) białek w tyreocytach u młodocianych pacjentów ze schorzeniami immunologicznymi i nieimmunologicznymi gruczołu tarczowego
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- Pediatric Endocrinology, Diabetes & Metabolism, 2007, v. 13, n. 2, p. 63
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- Article
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism.
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- 2017
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- Publication type:
- journal article
NKX2-5 Variant in Two Siblings with Thyroid Hemiagenesis.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 6, p. 3414, doi. 10.3390/ijms23063414
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- Article
Limited Mandibular Movements as a Consequence of Unilateral or Asymmetrical Temporomandibular Joint Involvement in Juvenile Idiopathic Arthritis Patients.
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- Journal of Clinical Medicine, 2020, v. 9, n. 8, p. 2576, doi. 10.3390/jcm9082576
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- Article
Treatment of cartilage-hair hypoplasia with recombinant human growth hormone.
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- Pediatrics International, 2013, v. 55, n. 6, p. e162, doi. 10.1111/ped.12215
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- Article
Ultrasound features of multinodular goiter in DICER1 syndrome.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-19709-0
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- Article
Molecular analysis of the corticotropin-releasing hormone receptor type 2 gene fragment in anorexia nervosa.
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- Archives of Psychiatry & Psychotherapy, 2009, v. 11, n. 2, p. 75
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- Article
Birth Weight in Different Etiologies of Disorders of Sex Development.
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- 2017
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- Publication type:
- journal article
Zespół Kawasakiego u dzieci z regionu Wielkopolski w dobie pierwszej fali pandemii COVID-19.
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- Paediatrics & Family Medicine / Pediatria i Medycyna Rodzinna, 2020, v. 16, n. 4, p. 396, doi. 10.15557/PiMR.2020.0071
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- Article
SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD).
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- Frontiers in Endocrinology, 2020, v. 11, p. 1, doi. 10.3389/fendo.2020.00368
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- Article
Pituitary Microsomal Autoantibodies in Patients with Childhood-Onset Combined Pituitary Hormone Deficiency: an Antigen Identification Attempt.
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- Archivum Immunologiae & Therapiae Experimentalis, 2016, v. 64, n. 6, p. 485, doi. 10.1007/s00005-016-0386-x
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- Article
Thyroid diseases in children and adolescents requiring surgical treatment--indications, techniques, results, and complications based on 10 years of the single center's own experience.
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- Frontiers in Endocrinology, 2024, p. 1, doi. 10.3389/fendo.2023.1301191
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- Article
Molecular Detection and Incidence of Y Chromosomal Material in Patients with Turner Syndrome.
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- Sexual Development, 2017, v. 11, n. 5/6, p. 254, doi. 10.1159/000484880
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- Article
Germ-line deletion in DICER1 revealed by a novel MLPA assay using synthetic oligonucleotides.
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- European Journal of Human Genetics, 2014, v. 22, n. 4, p. 564, doi. 10.1038/ejhg.2013.215
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- Article
The influence of growth hormone therapy on the cardiovascular system in Turner syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 11, p. 1363, doi. 10.1515/jpem-2020-0266
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- Publication type:
- Article
Autoimmune thyroid disease and allergic contact dermatitis: two immune-related pathologies in the same patient.
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- Journal of Pediatric Endocrinology & Metabolism, 2012, v. 25, n. 1/2, p. 31, doi. 10.1515/jpem-2011-0392
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- Publication type:
- Article
The usefulness of ultrasound in follow-up of a patient with dyshormonogenetic congenital hypothyroidism.
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- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 7/8, p. 549, doi. 10.1515/jpem.2011.180
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- Publication type:
- Article
Adrenal Function in Children with Severe Asthma Treated with High-Dose Inhaled Glucocorticoids: Recommended Screening Tests in Outpatient Conditions.
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- Journal of Pediatric Endocrinology & Metabolism, 2007, v. 20, n. 7, p. 781, doi. 10.1515/jpem.2007.20.7.781
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- Article
The Pediatric Outcomes Data Collection Instrument for a Polish sample with juvenile idiopathic arthritis: psychometric properties of proxy version.
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- International Journal of Rheumatic Diseases, 2017, v. 20, n. 12, p. 2077, doi. 10.1111/1756-185X.12738
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- Article
Analiza molekularna fragmentu genu dla drugiego typu receptora kortykoliberyny w jadłowstręcie psychicznym.
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- Psychiatria Polska, 2008, v. 42, n. 2, p. 209
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- Article
Uterine Development During Induced Puberty in Girls with Turner Syndrome.
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- Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.707031
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- Publication type:
- Article
Severe Hypothyroidism Due to Autoimmune Atrophic Thyroiditis - Predicted Target Height and a Plausible Mechanism for Sexual Precocity.
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- Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 7, p. 901, doi. 10.1515/jpem.2001.14.7.901
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- Article
Recurrent EZH1 mutations are a second hit in autonomous thyroid adenomas.
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- 2016
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- Publication type:
- journal article
X-Linked Adrenal Hypoplasia Congenita in a Boy due to a Novel Deletion of the Entire NR0B1 (DAX1) and MAGEB1–4 Genes.
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- International Journal of Endocrinology, 2016, p. 1, doi. 10.1155/2016/5178953
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- Publication type:
- Article
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.
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- BMC Pediatrics, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2431-13-27
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- Article
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.
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- 2013
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- Publication type:
- journal article
Autoimmune Thyroiditis Induced by Bartonella henselae (Cat-Scratch Disease) Might Be Reversible.
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- Pathobiology, 2023, v. 90, n. 2, p. 131, doi. 10.1159/000525399
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- Article
Mosaic IL6ST variant inducing constitutive GP130 cytokine receptor signaling as a cause of neonatal onset immunodeficiency with autoinflammation and dysmorphy.
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- Human Molecular Genetics, 2021, v. 30, n. 3/4, p. 226, doi. 10.1093/hmg/ddab035
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- Article
Evidence of a significant vitamin D deficiency among 9–13-year-old Polish children: results of a multicentre study.
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- European Journal of Nutrition, 2019, v. 58, n. 5, p. 2029, doi. 10.1007/s00394-018-1756-4
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- Article
The Usefulness of Magnetic Resonance Imaging of the Cardiovascular System in the Diagnostic Work-Up of Patients With Turner Syndrome.
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- Frontiers in Endocrinology, 2018, p. N.PAG, doi. 10.3389/fendo.2018.00609
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- Article
Multiples of Median-Transformed, Normalized Reference Ranges of Steroid Profiling Data Independent of Age, Sex, and Units.
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- Hormone Research in Paediatrics, 2018, v. 89, n. 4, p. 255, doi. 10.1159/000488028
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- Article
FOXE1 Polyalanine Tract Length Polymorphism in Patients with Thyroid Hemiagenesis and Subjects with Normal Thyroid.
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- Hormone Research in Paediatrics, 2011, v. 75, n. 5, p. 329, doi. 10.1159/000322874
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- Article
Genetic analysis of the PAPP-A2 gene and evaluation of free IGF-1, IGFBP-5, and ALS concentrations in a group of 22 patients with idiopathic short stature.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2024, v. 75, n. 4, p. 428, doi. 10.5603/ep.100030
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- Publication type:
- Article
X-linked hypophosphataemic rickets in children: clinical phenotype, therapeutic strategies, and molecular background.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2021, v. 72, n. 2, p. 108, doi. 10.5603/EP.a2020.0087
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- Publication type:
- Article
PAPP-A2 a new key regulator of growth.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2017, v. 68, n. 6, p. 682, doi. 10.5603/EP.a2017.0060
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- Article
PAPP-A2 nowy regulator procesu wzrastania.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2017, v. 68, n. 6, p. 687, doi. 10.5603/EP.a2017.0060
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- Publication type:
- Article
Diagnostics and treatment of differentiated thyroid carcinoma in children -- Guidelines of Polish National Societies.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2016, v. 67, n. 6, p. 628, doi. 10.5603/EP.2016.0072
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- Publication type:
- Article
The usefulness of the GHRH stimulation test in the diagnostics of growth hormone deficiency in children.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2015, v. 66, n. 2, p. 137, doi. 10.5603/EP.2015.0021
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- Publication type:
- Article
The role of the immune system and cytokines involved in the pathogenesis of autoimmune thyroid disease (AITD).
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2014, v. 65, n. 2, p. 150, doi. 10.5603/EP2014.0021
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- Publication type:
- Article
Diagnostyka i leczenie raka tarczycy u dzieci w Polsce w analizie wieloośrodkowej dla PPGGL.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2006, v. 57, n. Supplement A, p. A75
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- Publication type:
- Article
Mutations in proteasome-related genes are associated with thyroid hemiagenesis.
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- Endocrine (1355008X), 2017, v. 56, n. 2, p. 279, doi. 10.1007/s12020-017-1287-4
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- Article
ON THE LONGITUDINAL STRUCTURE FUNCTION IN THE DIPOLE MODEL.
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- Acta Physica Polonica B, 2015, v. 46, n. 10, p. 2019, doi. 10.5506/APhysPolB.46.2019
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- Article
Czy istnieje zależność między wartością wskaźnika masy ciała a astmą u dzieci?
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- Polish Pneumonology & Allergology / Pneumonologia i Alergologia Polska, 2008, v. 76, n. 2, p. 88
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- Publication type:
- Article
Autoimmune polyglandular syndrome type 2 in the form of Carpenter syndrome in a 16.5-year-old girl.
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- Polish Journal of Pediatrics / Pediatria Polska, 2024, v. 99, n. 1, p. 84, doi. 10.5114/polp.2024.135701
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- Publication type:
- Article