Works matching IS 13085727 AND DT 2021 AND VI 13 AND IP 1
Results: 15
Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 114, doi. 10.4274/jcrpe.galenos.2020.2020.0004
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6q25.1-q25.3 Microdeletion in a Chinese Girl.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 109, doi. 10.4274/jcrpe.galenos.2020.2020.0008
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The Unusual Case of Fibroma of Tendon Sheath in a Young Girl with Turner Syndrome Undergoing Growth Hormone Treatment.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 104, doi. 10.4274/jcrpe.galenos.2020.2019.0223
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Sirolimus Therapy and Follow-up in a Patient with Severe Congenital Hyperinsulinism Following Subtotal Pancreatectomy.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 119, doi. 10.4274/jcrpe.galenos.2020.2020.0033
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Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 100, doi. 10.4274/jcrpe.galenos.2020.2019.0213
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Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 88, doi. 10.4274/jcrpe.galenos.2020.2020.0132
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Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 80, doi. 10.4274/jcrpe.galenos.2020.2020.0093
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Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 72, doi. 10.4274/jcrpe.galenos.2020.2020.0108
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Transforming Growth Factor-β1 and Receptor for Advanced Glycation End Products Gene Expression and Protein Levels in Adolescents with Type 1 Diabetes Mellitus.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 61, doi. 10.4274/jcrpe.galenos.2020.2020.0155
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A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 52, doi. 10.4274/jcrpe.galenos.2020.2020.0101
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Very High Incidence of Type 1 Diabetes Among Children Aged Under 15 Years in Tlemcen, Northwest Algeria (2015-2018).
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 44, doi. 10.4274/jcrpe.galenos.2020.2020.0073
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Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 34, doi. 10.4274/jcrpe.galenos.2020.2020.0152
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Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 23, doi. 10.4274/jcrpe.galenos.2020.2020.0141
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Catch-up Growth in Prepubertal Children Treated for Juvenile Hypothyroidism and Growth Hormone Deficiency can be Modelled with a Monomolecular Function.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 15, doi. 10.4274/jcrpe.galenos.2020.2020.0130
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The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults.
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- Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 1, doi. 10.4274/jcrpe.galenos.2020.2019.0190
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