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 *

196 related articles for article (PubMed ID: 23518940)

  • 1. Bardet-Biedl syndrome and subaortic membrane: co-occurrence of two rare conditions.
    Arık OZ; Tekin K; Türkoğlu C; Çaylı M
    Turk Kardiyol Dern Ars; 2013 Jan; 41(1):55-8. PubMed ID: 23518940
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bardet-Biedl syndrome: a case series.
    Elawad OAMA; Dafallah MA; Ahmed MMM; Albashir AAD; Abdalla SMA; Yousif HHM; Daw Elbait AAE; Mohammed ME; Ali HIH; Ahmed MMM; Mohammed NFN; Osman FHM; Mohammed MAY; Abu Shama EAE
    J Med Case Rep; 2022 Apr; 16(1):169. PubMed ID: 35484558
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Clinical features of Bardet-Biedl syndrome with renal abnormalities as initial manifestations].
    Wang H; Fu Q; Shen Y; Liu X; Zhou N; Liang Y; Yao Y
    Zhonghua Er Ke Za Zhi; 2014 Aug; 52(8):611-5. PubMed ID: 25224240
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Second case of Bardet-Biedl syndrome caused by biallelic variants in IFT74.
    Kleinendorst L; Alsters SIM; Abawi O; Waisfisz Q; Boon EMJ; van den Akker ELT; van Haelst MM
    Eur J Hum Genet; 2020 Jul; 28(7):943-946. PubMed ID: 32144365
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child.
    Saida K; Inaba Y; Hirano M; Satake W; Toda T; Suzuki Y; Sudo A; Noda S; Hidaka Y; Hirabayashi K; Imai H; Kurokawa T; Koike K
    Brain Dev; 2014 Sep; 36(8):721-4. PubMed ID: 24290075
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Polydactyly and obesity - the clinical manifestation of ciliopathy: a boy with Bardet-Biedl syndrome.
    Szmigielska A; Krzemień G; Roszkowska-Blaim M; Obersztyn E
    Dev Period Med; 2016; 20(2):105-9. PubMed ID: 27442694
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pigmentary retinopathy due to Bardet-Biedl syndrome: case report and literature review.
    Andrade LJ; Andrade R; França CS; Bittencourt AV
    Arq Bras Oftalmol; 2009; 72(5):694-6. PubMed ID: 20027412
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bardet Biedl syndrome: A rare genetic disorder.
    Khan SA; Ahmad Ansari MZ; Khalid M
    J Pak Med Assoc; 2020 Sep; 70(9):1651-1652. PubMed ID: 33040131
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bardet-Biedl syndrome: a rare case report from North India.
    Kumar S; Mahajan BB; Mittal J
    Indian J Dermatol Venereol Leprol; 2012; 78(2):228. PubMed ID: 22421669
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of bifid epiglottis and laryngeal web with Bardet-Biedl syndrome: A case report.
    Poulin MA; Laframboise R; Blouin MJ
    Int J Pediatr Otorhinolaryngol; 2019 Jul; 122():138-140. PubMed ID: 31022684
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bardet-Biedl syndrome with syndrome X: a patient report.
    Keskin M; Atabek ME; Kurtoğlu S
    J Pediatr Endocrinol Metab; 2004 Jun; 17(6):913-5. PubMed ID: 15270411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two sisters with Bardet-Biedl syndrome: brain abnormalities and unusual facial findings.
    Aksoy A; Karagüzel G; Akbulut U; Türk A
    Turk J Pediatr; 2011; 53(4):460-3. PubMed ID: 21980853
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey.
    Beales PL; Elcioglu N; Woolf AS; Parker D; Flinter FA
    J Med Genet; 1999 Jun; 36(6):437-46. PubMed ID: 10874630
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bardet-Biedl syndrome a rare cause of cardiomyopathy.
    Yadav DK; Beniwal MK; Jain A
    Indian Pediatr; 2013 Jun; 50(6):599-601. PubMed ID: 23942403
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cerebellar vermis hypoplasia in a patient with Bardet-Biedl syndrome.
    Baskin E; Kayiran SM; Oto S; Alehan F; Agildere AM; Saatçi U
    J Child Neurol; 2002 May; 17(5):385-7. PubMed ID: 12150587
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bardet-Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene.
    Morohashi T; Hayashi T; Mizobuchi K; Nakano T; Morioka I
    Doc Ophthalmol; 2023 Apr; 146(2):165-171. PubMed ID: 36574078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Laurence Moon Bardet Biedl Syndrome.
    Abdulla AB; Niloy AA; Shah TA; Biswas SK; Imran AK; Murshed KM; Ahmed M
    Mymensingh Med J; 2009 Jan; 18(1 Suppl):S124-128. PubMed ID: 19377420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bardet-biedl syndrome and brain abnormalities.
    Rooryck C; Pelras S; Chateil JF; Cances C; Arveiler B; Verloes A; Lacombe D; Goizet C
    Neuropediatrics; 2007 Feb; 38(1):5-9. PubMed ID: 17607597
    [TBL] [Abstract][Full Text] [Related]  

  • 19. C8orf37 is mutated in Bardet-Biedl syndrome and constitutes a locus allelic to non-syndromic retinal dystrophies.
    Khan AO; Decker E; Bachmann N; Bolz HJ; Bergmann C
    Ophthalmic Genet; 2016 Sep; 37(3):290-3. PubMed ID: 26854863
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Patient with Bardet-Biedl syndrome presenting with nystagmus at fifteen months of age.
    Musarella MA
    J AAPOS; 2001 Aug; 5(4):262-4. PubMed ID: 11507589
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.