BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 32248673)

  • 1. A Case Report of Pycnodysostosis Associated with Multiple Pituitary Hormone Deficiencies and Response to Treatment.
    Verma V; Singh RK
    J Clin Res Pediatr Endocrinol; 2020 Nov; 12(4):444-449. PubMed ID: 32248673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evaluation of Clinical Characteristics and Growth Hormone Response in a Rare Skeletal Dysplasia: Pycnodysostosis.
    Ünsal Y; Atar S
    Cureus; 2023 Sep; 15(9):e44823. PubMed ID: 37809147
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pycnodysostosis: clinical, radiologic, and endocrine evaluation and linear growth after growth hormone therapy.
    Soliman AT; Ramadan MA; Sherif A; Aziz Bedair ES; Rizk MM
    Metabolism; 2001 Aug; 50(8):905-11. PubMed ID: 11474477
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and genetic evaluation of Danish patients with pycnodysostosis.
    Doherty MA; Langdahl BL; Vogel I; Haagerup A
    Eur J Med Genet; 2021 Feb; 64(2):104135. PubMed ID: 33429075
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Short stature Revealing a Pycnodysostosis: A Case Report.
    Aynaou H; Skiker I; Latrech H
    J Orthop Case Rep; 2016; 6(2):43-45. PubMed ID: 27703936
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pathological mandibular fracture complicated by osteonecrosis in an adult patient with pycnodysostosis: clinical report and review of the literature.
    Moroni A; Brizola E; Di Cecco A; Tremosini M; Sergiampietri M; Bianchi A; Tappino B; Piana M; Gnoli M
    Eur J Med Genet; 2024 Feb; 67():104904. PubMed ID: 38141876
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A Pediatric Case of Xanthogranuloma in the Suprasellar Region Detected by a Severe Short Stature after 6 Years Growth Failure].
    Shimamoto T; Yamamoto Y; Kuwamura M; Asai H; Ishii M; Honda Y; Kusuhara K
    J UOEH; 2019; 41(2):249-257. PubMed ID: 31292372
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pycnodysostosis with novel gene mutation and sporadic medullary thyroid carcinoma: A case report.
    Shi X; Huang C; Xiao F; Liu W; Zeng J; Li X
    Medicine (Baltimore); 2017 Dec; 96(50):e8730. PubMed ID: 29390266
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ichthyosis vulgaris and pycnodysostosis: an unusual occurrence.
    Kshirsagar VY; Ahmed M; Nagarsenkar S; Sahoo K; Shah KB
    Acta Med Acad; 2012; 41(2):214-8. PubMed ID: 23331396
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Autosomal recessive deficiency of combined pituitary hormones (except ACTH) in a consanguineous Brazilian kindred.
    Nogueira CR; Leite CC; Chedid EP; Liberman B; Pimentel-Filho FR; Kopp P; Medeiros-Neto GA
    J Endocrinol Invest; 1997 Nov; 20(10):629-33. PubMed ID: 9438923
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pycnodysostosis at otorhinolaryngology.
    Baglam T; Binnetoglu A; Fatih Topuz M; Baş Ikizoglu N; Ersu R; Turan S; Sarı M
    Int J Pediatr Otorhinolaryngol; 2017 Apr; 95():91-96. PubMed ID: 28576543
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pycnodysostosis- a rare disorder with distinctive craniofacial dysmorphia. A case report.
    Sharma A; Upmanyu A; Parate AR; Kasat VO
    J Oral Biol Craniofac Res; 2021; 11(4):529-535. PubMed ID: 34377661
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency.
    Boda H; Miyata M; Inagaki H; Shinkai Y; Kato T; Yoshikawa T; Kurahashi H
    Eur J Med Genet; 2019 Nov; 62(11):103570. PubMed ID: 30414530
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recombinant hGH replacement therapy and the hypothalamus-pituitary-thyroid axis in children with GH deficiency: when should we be concerned about the occurrence of central hypothyroidism?
    Giavoli C; Porretti S; Ferrante E; Cappiello V; Ronchi CL; Travaglini P; Epaminonda P; Arosio M; Beck-Peccoz P
    Clin Endocrinol (Oxf); 2003 Dec; 59(6):806-10. PubMed ID: 14974926
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Long-Term Outcomes, Genetics, and Pituitary Morphology in Patients with Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiencies: A Single-Centre Experience of Four Decades of Growth Hormone Replacement.
    Rohayem J; Drechsel H; Tittel B; Hahn G; Pfaeffle R; Huebner A
    Horm Res Paediatr; 2016; 86(2):106-116. PubMed ID: 27487097
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect.
    Otaify GA; Abdel-Hamid MS; Mehrez MI; Aboul-Ezz E; Zaki MS; Aglan MS; Temtamy SA
    Osteoporos Int; 2018 Aug; 29(8):1833-1841. PubMed ID: 29796728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical and genetic aspects of combined pituitary hormone deficiencies].
    Castinetti F; Reynaud R; Saveanu A; Quentien MH; Albarel F; Barlier A; Enjalbert A; Brue T
    Ann Endocrinol (Paris); 2008 Feb; 69(1):7-17. PubMed ID: 18291347
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A child with bone fractures and dysmorphic features: remember of pycnodysostosis and craniosynostosis.
    Berenguer A; Freitas AP; Ferreira G; Nunes JL
    BMJ Case Rep; 2012 Nov; 2012():. PubMed ID: 23175007
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-term effects of growth hormone (GH) on bone mineral status and bone turnover markers in patients with isolated GH deficiency and multiple pituitary hormone deficiency.
    Gonc EN; Kandemir N
    Clin Endocrinol (Oxf); 2007 May; 66(5):672-7. PubMed ID: 17381489
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pituitary hyperplasia in children with short stature and primary hypothyroidism.
    Aijing X; Tang L
    Indian Pediatr; 2010 Oct; 47(10):877-80. PubMed ID: 20453264
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.