These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 28720553)

  • 1. Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor Deletion.
    Mahmoud R; Naidu A; Risheg H; Kimonis V
    J Clin Res Pediatr Endocrinol; 2017 Dec; 9(4):380-386. PubMed ID: 28720553
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome.
    Tamura T; Tohma T; Ohta T; Soejima H; Harada N; Abe K; Niikawa N
    Clin Dysmorphol; 1993 Apr; 2(2):106-13. PubMed ID: 7506614
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Successful long-term growth hormone therapy in a girl with haploinsufficiency of the insulin-like growth factor-I receptor due to a terminal 15q26.2->qter deletion detected by multiplex ligation probe amplification.
    Walenkamp MJ; de Muinck Keizer-Schrama SM; de Mos M; Kalf ME; van Duyvenvoorde HA; Boot AM; Kant SG; White SJ; Losekoot M; Den Dunnen JT; Karperien M; Wit JM
    J Clin Endocrinol Metab; 2008 Jun; 93(6):2421-5. PubMed ID: 18349070
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Increasing knowledge in
    Giabicani E; Willems M; Steunou V; Chantot-Bastaraud S; Thibaud N; Abi Habib W; Azzi S; Lam B; Bérard L; Bony-Trifunovic H; Brachet C; Brischoux-Boucher E; Caldagues E; Coutant R; Cuvelier ML; Gelwane G; Guemas I; Houang M; Isidor B; Jeandel C; Lespinasse J; Naud-Saudreau C; Jesuran-Perelroizen M; Perrin L; Piard J; Sechter C; Souchon PF; Storey C; Thomas D; Le Bouc Y; Rossignol S; Netchine I; Brioude F
    J Med Genet; 2020 Mar; 57(3):160-168. PubMed ID: 31586944
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three novel IGF1R mutations in microcephalic patients with prenatal and postnatal growth impairment.
    Juanes M; Guercio G; Marino R; Berensztein E; Warman DM; Ciaccio M; Gil S; Bailez M; Rivarola MA; Belgorosky A
    Clin Endocrinol (Oxf); 2015 May; 82(5):704-11. PubMed ID: 25040157
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene.
    Roback EW; Barakat AJ; Dev VG; Mbikay M; Chrétien M; Butler MG
    Am J Med Genet; 1991 Jan; 38(1):74-9. PubMed ID: 1849352
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Growth in individuals with Majewski osteodysplastic primordial dwarfism type II caused by pericentrin mutations.
    Bober MB; Niiler T; Duker AL; Murray JE; Ketterer T; Harley ME; Alvi S; Flora C; Rustad C; Bongers EM; Bicknell LS; Wise C; Jackson AP
    Am J Med Genet A; 2012 Nov; 158A(11):2719-25. PubMed ID: 22821869
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterozygous nonsense mutations near the C-terminal region of IGF1R in two patients with small-for-gestational-age-related short stature.
    Fujimoto M; Kawashima Sonoyama Y; Hamajima N; Hamajima T; Kumura Y; Miyahara N; Nishimura R; Adachi K; Nanba E; Hanaki K; Kanzaki S
    Clin Endocrinol (Oxf); 2015 Dec; 83(6):834-41. PubMed ID: 25866162
    [TBL] [Abstract][Full Text] [Related]  

  • 9. IGF1R Variants in Patients With Growth Impairment: Four Novel Variants and Genotype-Phenotype Correlations.
    Yang L; Xu DD; Sun CJ; Wu J; Wei HY; Liu Y; Zhang MY; Luo FH
    J Clin Endocrinol Metab; 2018 Nov; 103(11):3939-3944. PubMed ID: 30053089
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Persistent short stature, other potential outcomes, and the effect of growth hormone treatment in children who are born small for gestational age.
    Lee PA; Kendig JW; Kerrigan JR
    Pediatrics; 2003 Jul; 112(1 Pt 1):150-62. PubMed ID: 12837881
    [No Abstract]   [Full Text] [Related]  

  • 11. Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay.
    Witsch J; Szafranski P; Chen CA; Immken L; Simpson Patel G; Hixson P; Cheung SW; Stankiewicz P; Schaaf CP
    Eur J Hum Genet; 2013 Nov; 21(11):1304-7. PubMed ID: 23486542
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2.
    Vasques GA; Hisado-Oliva A; Funari MF; Lerario AM; Quedas EP; Solberg P; Heath KE; Jorge AA
    J Pediatr Endocrinol Metab; 2017 Jan; 30(1):111-116. PubMed ID: 27941173
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Neurocognitive and psychosocial development in SGA and the indication for growth hormone therapy].
    Noeker M
    Klin Padiatr; 2006; 218(5):249-59. PubMed ID: 16947092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microdeletion in the IGF-1 receptor gene of a patient with short stature and obesity: a case report.
    Yoon JS; Hwang IT
    J Pediatr Endocrinol Metab; 2021 Feb; 34(2):255-259. PubMed ID: 33544498
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the clinical spectrum of chromosome 15q26 terminal deletions associated with IGF-1 resistance.
    O'Riordan AM; McGrath N; Sharif F; Murphy NP; Franklin O; Lynch SA; O'Grady MJ
    Eur J Pediatr; 2017 Jan; 176(1):137-142. PubMed ID: 27826649
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Growth hormone regimens in Australia: analysis of the first 3 years of treatment for idiopathic growth hormone deficiency and idiopathic short stature.
    Hughes IP; Harris M; Choong CS; Ambler G; Cutfield W; Hofman P; Cowell CT; Werther G; Cotterill A; Davies PS;
    Clin Endocrinol (Oxf); 2012 Jul; 77(1):62-71. PubMed ID: 21950731
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic IGF1R defects: new cases expand the spectrum of clinical features.
    Gonc EN; Ozon ZA; Oguz S; Kabacam S; Taskiran EZ; Kiper POS; Utine GE; Alikasifoglu A; Kandemir N; Boduroglu OK; Alikasifoglu M
    J Endocrinol Invest; 2020 Dec; 43(12):1739-1748. PubMed ID: 32356191
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Successful Growth Hormone Therapy in Cornelia de Lange Syndrome.
    de Graaf M; Kant SG; Wit JM; Willem Redeker EJ; Eduard Santen GW; Henriëtta Verkerk AJM; Uitterlinden AG; Losekoot M; Oostdijk W
    J Clin Res Pediatr Endocrinol; 2017 Dec; 9(4):366-370. PubMed ID: 28588001
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The future of research into growth hormone responsiveness.
    Rosenfeld RG
    Horm Res; 2009 Apr; 71 Suppl 2():71-4. PubMed ID: 19407500
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF-I receptor (IGF1R) gene.
    Labarta JI; Barrio E; Audí L; Fernández-Cancio M; Andaluz P; de Arriba A; Puga B; Calvo MT; Mayayo E; Carrascosa A; Ferrández-Longás A
    Clin Endocrinol (Oxf); 2013 Feb; 78(2):255-62. PubMed ID: 22738321
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.