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 *

166 related articles for article (PubMed ID: 32621723)

  • 41. Phenotype-genotype correlations in congenital isolated growth hormone deficiency (IGHD).
    Alatzoglou KS; Dattani MT
    Indian J Pediatr; 2012 Jan; 79(1):99-106. PubMed ID: 22139958
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A heterozygous microdeletion of 20p12.2-3 encompassing PROKR2 and BMP2 in a patient with congenital hypopituitarism and growth hormone deficiency.
    Parsons SJH; Wright NB; Burkitt-Wright E; Skae MS; Murray PG
    Am J Med Genet A; 2017 Aug; 173(8):2261-2267. PubMed ID: 28586151
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The molecular basis of hypopituitarism.
    Romero CJ; Nesi-França S; Radovick S
    Trends Endocrinol Metab; 2009 Dec; 20(10):506-16. PubMed ID: 19854060
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Neuroradiological investigation in patients with idiopathic growth hormone deficiency].
    Bordallo MA; Tellerman LD; Bosignoli R; Oliveira FF; Gazolla FM; Madeira IR; Zanier JF; Henriques JL
    J Pediatr (Rio J); 2004; 80(3):223-8. PubMed ID: 15192766
    [TBL] [Abstract][Full Text] [Related]  

  • 45. MR findings in hereditary isolated growth hormone deficiency.
    Kornreich L; Horev G; Lazar L; Josefsberg Z; Pertzelan A
    AJNR Am J Neuroradiol; 1997 Oct; 18(9):1743-7. PubMed ID: 9367326
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Pathogenesis and Diagnosis of Growth Hormone Deficiency in Adults.
    Melmed S
    N Engl J Med; 2019 Jun; 380(26):2551-2562. PubMed ID: 31242363
    [No Abstract]   [Full Text] [Related]  

  • 47. Growth without growth hormone and similar dysmorphic features in three patients with sporadic combined pituitary hormone deficiencies.
    Gat-Yablonski G; Lazar L; Bar M; de Vries L; Weintrob N; Phillip M
    Horm Res; 2009; 72(5):302-9. PubMed ID: 19844116
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Unusual and lesser-known rare causes of adult growth hormone deficiency.
    Das L; Dutta P
    Best Pract Res Clin Endocrinol Metab; 2023 Dec; 37(6):101820. PubMed ID: 37704550
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type II.
    Kempers MJ; van der Crabben SN; de Vroede M; Alfen-van der Velden J; Netea-Maier RT; Duim RA; Otten BJ; Losekoot M; Wit JM
    Horm Res Paediatr; 2013; 80(6):390-6. PubMed ID: 24280736
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Effects of short term growth hormone therapy in adult growth hormone deficiency.
    Dutta P; Bhansali A; Ajith Kumar BV; Sharma R; Jaggi S; Bhadada S
    J Assoc Physicians India; 2010 Nov; 58():670-3. PubMed ID: 21510459
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Systematic profiling of clinical missence mutation effects on the intermolecular interaction between human growth hormone and its receptor in isolated growth hormone deficiency.
    Liu H; Xu L; Huang H; Zhao P; Yang R; Zhou Q; Liu G
    J Mol Graph Model; 2019 Nov; 92():1-7. PubMed ID: 31279174
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Characterization of a Novel POU1F1 Mutation Identified on Screening 160 Growth Hormone Deficiency Patients.
    Birla S; Vijayakumar P; Sehgal S; Bhatnagar S; Pallavi K; Sharma A
    Horm Metab Res; 2019 Apr; 51(4):248-255. PubMed ID: 31022740
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Rational use of the laboratory for childhood and adult growth hormone deficiency.
    Pandian R; Nakamoto JM
    Clin Lab Med; 2004 Mar; 24(1):141-74. PubMed ID: 15157561
    [TBL] [Abstract][Full Text] [Related]  

  • 55. De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?
    Massa GG; Binder G; Oostdijk W; Ranke MB; Wit JM
    Eur J Pediatr; 1998 Apr; 157(4):272-5. PubMed ID: 9578959
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Neuroradiologic diagnosis of the hypothalamo-hypophyseal region in children with hypopituitarism].
    Di Natale B; De Angelis R; Lukezic M; Pellini C; Chiumello G
    Minerva Endocrinol; 1993 Sep; 18(3 Suppl 1):48-52. PubMed ID: 8190047
    [No Abstract]   [Full Text] [Related]  

  • 57. Mutations in PROP1 cause familial combined pituitary hormone deficiency.
    Wu W; Cogan JD; Pfäffle RW; Dasen JS; Frisch H; O'Connell SM; Flynn SE; Brown MR; Mullis PE; Parks JS; Phillips JA; Rosenfeld MG
    Nat Genet; 1998 Feb; 18(2):147-9. PubMed ID: 9462743
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Growth hormone of dried blood spot for the diagnosis of growth hormone deficiency].
    Domínguez-Menéndez G; Cifuentes L; González C; Lagos M; Quiroga T; Rumié H; Torres C; Martínez-Aguayo A
    Rev Chil Pediatr; 2019 Apr; 90(2):145-151. PubMed ID: 31095230
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The prevalence of growth hormone deficiency in survivors of subarachnoid haemorrhage: results from a large single centre study.
    Giritharan S; Cox J; Heal CJ; Hughes D; Gnanalingham K; Kearney T
    Pituitary; 2017 Dec; 20(6):624-634. PubMed ID: 28822018
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Growth hormone (GH-1) gene deletions in children with isolated growth hormone deficiency (IGHD).
    Desai MP; Mithbawkar SM; Upadhye PS; Shalia KK
    Indian J Pediatr; 2012 Jul; 79(7):875-83. PubMed ID: 22016154
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.