Works matching Pituitary hormones


Results: 5000
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    Congenital pituitary hormone deficiencies: role of LHX3/LHX4 genes.

    Published in:
    Expert Review of Endocrinology & Metabolism, 2008, v. 3, n. 6, p. 751, doi. 10.1586/17446651.3.6.751
    By:
    • Castinetti, Frederic;
    • Reynaud, Rachel;
    • Saveanu, Alexandru;
    • Quentien, Marie-Helene;
    • Albarel, Frederique;
    • Enjalbert, Alain;
    • Barlier, Anne;
    • Brue, Thierry
    Publication type:
    Article
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    PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 4, p. 338, doi. 10.4274/jcrpe.galenos.2023.2023-4-4
    By:
    • Kardelen, Aslı Derya;
    • Najaflı, Adam;
    • Baş, Firdevs;
    • Karaman, Birsen;
    • Toksoy, Güven;
    • Poyrazoğlu, Şükran;
    • Avcı, Şahin;
    • Altunoğlu, Umut;
    • Abalı, Zehra Yavaş;
    • Öztürk, Ayşe Pınar;
    • Özturan, Esin Karakılıç;
    • Başaran, Seher;
    • Darendeliler, Feyza;
    • Uyguner, Z. Oya
    Publication type:
    Article
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    Comparison of response to 2-years' growth hormone treatment in children with isolated growth hormone deficiency, born small for gestational age, idiopathic short stature, or multiple pituitary hormone deficiency: combined results from two large observational studies

    Published in:
    International Journal of Pediatric Endocrinology, 2012, p. 1, doi. 10.1186/1687-9856-2012-22
    By:
    • Peter A. Lee;
    • Sävendahl, Lars;
    • Oliver, Isabelle;
    • Tauber, Maithé;
    • Blankenstein, Oliver;
    • Ross, Judith;
    • Snajderova, Marta;
    • Rakov, Viatcheslav;
    • Tønnes Pedersen, Birgitte;
    • Christesen, Henrik Thybo
    Publication type:
    Article
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    Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.

    Published in:
    Clinical Endocrinology, 2017, v. 87, n. 6, p. 725, doi. 10.1111/cen.13430
    By:
    • Madeira, Joao LO;
    • Nishi, Mirian Y;
    • Nakaguma, Marilena;
    • Benedetti, Anna F;
    • Biscotto, Isabela Peixoto;
    • Fernandes, Thamiris;
    • Pequeno, Thiago;
    • Figueiredo, Thalita;
    • Franca, Marcela M;
    • Correa, Fernanda A;
    • Otto, Aline P;
    • Abrão, Milena;
    • Miras, Mirta B;
    • Santos, Silvana;
    • Jorge, Alexander AL;
    • Costalonga, Everlayny F;
    • Mendonca, Berenice B;
    • Arnhold, Ivo JP;
    • Carvalho, Luciani R
    Publication type:
    Article
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    A Novel Missense Variant in LHX4 in Three Children with Multiple Pituitary Hormone Deficiency Belonging to Two Unrelated Families and Contribution of Additional GLI2 and IGFR1 Variant.

    Published in:
    Children, 2025, v. 12, n. 3, p. 364, doi. 10.3390/children12030364
    By:
    • Santoro, Claudia;
    • Aiello, Francesca;
    • Farina, Antonella;
    • Miraglia del Giudice, Emanuele;
    • Pascarella, Filomena;
    • Licenziati, Maria Rosaria;
    • Improda, Nicola;
    • Piluso, Giulio;
    • Torella, Annalaura;
    • Del Vecchio Blanco, Francesca;
    • Cirillo, Mario;
    • Nigro, Vincenzo;
    • Grandone, Anna
    Publication type:
    Article
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