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 *

100 related articles for article (PubMed ID: 7584699)

  • 1. Hypopituitarism and chorioretinopathy in two siblings.
    Wu R; Ling C; Hahn YS
    J Pediatr Endocrinol Metab; 1995; 8(1):55-9. PubMed ID: 7584699
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chorioretinopathy and pituitary dysfunction. The CPD syndrome.
    Judisch GF; Lowry RB; Hanson JW; McGillivary BC
    Arch Ophthalmol; 1981 Feb; 99(2):253-6. PubMed ID: 7469861
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiple pituitary hormone deficiencies in eight siblings of one Jewish Moroccan family.
    Adler-Bier M; Pertzeland A; Laron Z; Lieberman E; Moses S
    Acta Paediatr Scand; 1979 May; 68(3):401-4. PubMed ID: 220839
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Electroretinograms in microcephaly with chorioretinal degeneration.
    Manning FJ; Bruce AM; Berson EL
    Am J Ophthalmol; 1990 Apr; 109(4):457-63. PubMed ID: 2330949
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial hypopituitarism associated with mosaic form of Turner syndrome.
    Lomna-Bogdanov E; Bolanowski M; Slezak R; Sokolska V; Pałczyiński B; Spring A; Demissie M
    Gynecol Endocrinol; 2005 Jan; 20(1):22-5. PubMed ID: 15969242
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Are hypersegmented neutrophils a characteristic of Boucher-Neuhäuser syndrome?
    Umehara T; Yaguchi H; Suzuki M; Isozaki E; Mochio S
    J Neurol Sci; 2010 Aug; 295(1-2):128-30. PubMed ID: 20605169
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Report of a novel lobular chorioretinal dystrophy.
    Moradi P; Lotery A
    Eye (Lond); 2006 Dec; 20(12):1390-2. PubMed ID: 16456598
    [No Abstract]   [Full Text] [Related]  

  • 8. Familial congenital hypopituitarism with central diabetes insipidus.
    Yagi H; Nagashima K; Miyake H; Tamai S; Onigata K; Yutani S; Kuroume T
    J Clin Endocrinol Metab; 1994 Apr; 78(4):884-9. PubMed ID: 8157716
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variable X-linked recessive hypopituitarism with evidence of gonadotropin deficiency in two pre-pubertal males.
    Zipf WB; Kelch RP; Bacon GE
    Clin Genet; 1977 Apr; 11(4):249-54. PubMed ID: 192503
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Posterior cystoid retinal degeneration in central serous chorioretinopathy.
    Piccolino FC; De La Longrais RR; Manea M; Cicinelli S
    Retina; 2008; 28(7):1008-12. PubMed ID: 18698305
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The combined pituitary function test in children: an evaluation of the clinical usefulness of TRH and LHRH stimulation tests through a retrospective analysis of one hundred and twenty six cases.
    Westwood ME; Butler GE; McLellan AC; Barth JH
    Clin Endocrinol (Oxf); 2000 Jun; 52(6):727-33. PubMed ID: 10848877
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Closure of a full-thickness macular hole without vitrectomy in choroideraemia.
    Ishikawa K; Gekka T; Hayashi T; Kikuchi S; Kameya S; Tsuneoka H
    Clin Exp Optom; 2017 May; 100(3):294-295. PubMed ID: 27628750
    [No Abstract]   [Full Text] [Related]  

  • 13. Growth hormone deficiency in two siblings with Alström syndrome.
    Alter CA; Moshang T
    Am J Dis Child; 1993 Jan; 147(1):97-9. PubMed ID: 8418611
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hypogonadotrophic hypogonadism, short stature, cerebellar ataxia, rod-cone retinal dystrophy, and hypersegmented neutrophils: a novel disorder or a new variant of Boucher-Neuhauser syndrome?
    Jbour AK; Mubaidin AF; Till M; El-Shanti H; Hadidi A; Ajlouni KM
    J Med Genet; 2003 Jan; 40(1):e2. PubMed ID: 12525550
    [No Abstract]   [Full Text] [Related]  

  • 15. 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; 1998 Jun; 21(6):386-91. PubMed ID: 9699131
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Peripheral vitreochorioretinal dystrophies and retinal detachment in pregnant women: diagnosis, treatment, and choice of a delivery procedure].
    Krasnoshchekova EE; Pankrushova TG; Boĭko EV
    Vestn Oftalmol; 2009; 125(2):40-2. PubMed ID: 19517831
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: possible familial RHYNS syndrome.
    Hedera P; Gorski JL
    Am J Med Genet; 2001 Jun; 101(2):142-5. PubMed ID: 11391657
    [TBL] [Abstract][Full Text] [Related]  

  • 19. HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.
    Fang Q; Benedetti AF; Ma Q; Gregory L; Li JZ; Dattani M; Sadeghi-Nejad A; Arnhold IJ; Mendonca BB; Camper SA; Carvalho LR
    Clin Endocrinol (Oxf); 2016 Sep; 85(3):408-14. PubMed ID: 27000987
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hallermann-Streiff syndrome with hypopituitarism contributing to growth failure.
    Pivnick EK; Burstein S; Wilroy RS; Kaufman RA; Ward JC
    Am J Med Genet; 1991 Dec; 41(4):503-7. PubMed ID: 1776645
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.