BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

60 related articles for article (PubMed ID: 9632165)

  • 1. Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency.
    Fofanova OV; Takamura N; Kinoshita E; Yoshimoto M; Tsuji Y; Peterkova VA; Evgrafov OV; Dedov II; Goncharov NP; Yamashita S
    Am J Med Genet; 1998 Jun; 77(5):360-5. PubMed ID: 9632165
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The clinical presentation of PIT1 positive pituitary neuroendocrine tumor immunonegative for growth hormone, prolactin, and thyroid stimulating hormone with analysis of clinical and immunostaining dissociation.
    Hong S; Shinya Y; Trejo-Lopez JA; Gruber LM; Erickson D; Bendok BR; Chaichana KL; Atkinson JL; Marino MJ; Donaldson AM; Stokken JK; Westphal SA; Chang AY; Samson SL; Choby GW; Van Gompel JJ
    Clin Neurol Neurosurg; 2024 Jan; 236():108075. PubMed ID: 38056042
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT).
    Nose O; Tatsumi K; Nakano Y; Amino N
    J Pediatr Endocrinol Metab; 2006 Apr; 19(4):491-8. PubMed ID: 16759034
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Kardelen AD; Najafli A; Baş F; Karaman B; Toksoy G; Poyrazoğlu Ş; Avcı Ş; Altunoğlu U; Yavaş Abalı Z; Öztürk AP; Karakılıç Özturan E; Başaran S; Darendeliler F; Uyguner ZO
    J Clin Res Pediatr Endocrinol; 2023 Nov; 15(4):338-347. PubMed ID: 37338295
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High
    Kardelen AD; Karakılıç Özturan E; Poyrazoğlu Ş; Baş F; Ceylaner S; Joustra SD; Wit JM; Darendeliler F
    J Clin Res Pediatr Endocrinol; 2023 Nov; 15(4):431-437. PubMed ID: 35466665
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Plurihormonal PIT1-lineage pituitary neuroendocrine tumors: a clinicopathological study].
    Duan ZJ; Feng J; Zhao HQ; Wang HD; Gui QP; Zhang XF; Ma Z; Hu ZJ; Xiang L; Qi XL
    Zhonghua Bing Li Xue Za Zhi; 2023 Oct; 52(10):1017-1024. PubMed ID: 37805393
    [No Abstract]   [Full Text] [Related]  

  • 7. Digital image analysis allows objective stratification of patients with silent PIT1-lineage pituitary neuroendocrine tumors.
    Zhao J; Ji C; Cheng H; Ye Z; Yao B; Shen M; Shou X; Zhou X; Ye H; Zhang Z; Chen H; Wang Y; He F; Zhao Y; Gong W; Zhang Q; Qiao N
    J Pathol Clin Res; 2023 Nov; 9(6):488-497. PubMed ID: 37661840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Growth hormone - 30 years of clinical practice: past, present, future].
    Dedov II; Bezlepkina OB; Pankratova MS; Nagaeva EV; Raykina EN; Peterkova VA
    Probl Endokrinol (Mosk); 2024 Feb; 70(1):4-12. PubMed ID: 38433536
    [TBL] [Abstract][Full Text] [Related]  

  • 9. POU1F1/Pou1f1 c.143-83A > G Variant Disrupts the Branch Site in Pre-mRNA and Leads to Dwarfism.
    Akiba K; Hasegawa Y; Katoh-Fukui Y; Terao M; Takada S; Hasegawa T; Fukami M; Narumi S
    Endocrinology; 2022 Dec; 164(2):. PubMed ID: 36427334
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Novel Splice-Site Deletion in the
    Hassan SS; Abdullah M; Trebusak Podkrajsek K; Musa S; Ibrahim A; Babiker O; Kovac J; Battelino T; Avbelj Stefanija M
    Genes (Basel); 2022 Apr; 13(4):. PubMed ID: 35456463
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital hypopituitarism due to novel compound heterozygous
    Chen WY; Niu DM; Chen LZ; Yang CF
    Mol Genet Metab Rep; 2021 Dec; 29():100819. PubMed ID: 34815942
    [TBL] [Abstract][Full Text] [Related]  

  • 12. POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature.
    Jadhav S; Diwaker C; Lila AR; Gada JV; Kale S; Sarathi V; Thadani PM; Arya S; Patil VA; Shah NS; Bandgar TR
    Pituitary; 2021 Oct; 24(5):657-669. PubMed ID: 33742319
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extreme Short Stature and Severe Neurological Impairment in a 17-Year-Old Male With Untreated Combined Pituitary Hormone Deficiency Due to
    Majdoub H; Amselem S; Legendre M; Rath S; Bercovich D; Tenenbaum-Rakover Y
    Front Endocrinol (Lausanne); 2019; 10():381. PubMed ID: 31316460
    [No Abstract]   [Full Text] [Related]  

  • 14. Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism.
    Pérez Millán MI; Vishnopolska SA; Daly AZ; Bustamante JP; Seilicovich A; Bergadá I; Braslavsky D; Keselman AC; Lemons RM; Mortensen AH; Marti MA; Camper SA; Kitzman JO
    Mol Genet Genomic Med; 2018 May; 6(4):514-25. PubMed ID: 29739035
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital hypopituitarism: how to select the patients for genetic analyses.
    Crisafulli G; Aversa T; Zirilli G; De Luca F; Gallizzi R; Wasniewska M
    Ital J Pediatr; 2018 Apr; 44(1):47. PubMed ID: 29625578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.
    Fang Q; George AS; Brinkmeier ML; Mortensen AH; Gergics P; Cheung LY; Daly AZ; Ajmal A; Pérez Millán MI; Ozel AB; Kitzman JO; Mills RE; Li JZ; Camper SA
    Endocr Rev; 2016 Dec; 37(6):636-675. PubMed ID: 27828722
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD.
    Sobrier ML; Tsai YC; Pérez C; Leheup B; Bouceba T; Duquesnoy P; Copin B; Sizova D; Penzo A; Stanger BZ; Cooke NE; Liebhaber SA; Amselem S
    Hum Mol Genet; 2016 Feb; 25(3):472-83. PubMed ID: 26612202
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic regulation of pituitary gland development in human and mouse.
    Kelberman D; Rizzoti K; Lovell-Badge R; Robinson IC; Dattani MT
    Endocr Rev; 2009 Dec; 30(7):790-829. PubMed ID: 19837867
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency.
    Carlomagno Y; Salerno M; Vivenza D; Capalbo D; Godi M; Mellone S; Tiradani L; Corneli G; Momigliano-Richiardi P; Bona G; Giordano M
    J Endocrinol Invest; 2009 Sep; 32(8):653-8. PubMed ID: 19498317
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency.
    Fofanova OV; Takamura N; Kinoshita E; Parks JS; Brown MR; Peterkova VA; Evgrafov OV; Goncharov NP; Bulatov AA; Dedov II; Yamashita S
    Pituitary; 1998 Apr; 1(1):45-9. PubMed ID: 11081182
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.