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 *

182 related articles for article (PubMed ID: 26055589)

  • 1. Characteristics of 22q 11.2 deletion syndrome undiagnosed until adulthood: an example suggesting the importance of psychiatric manifestations.
    Furuya K; Sasaki Y; Takeuchi T; Urita Y
    BMJ Case Rep; 2015 Jun; 2015():. PubMed ID: 26055589
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Rare Etiology of Hypocalcemic Seizures in Adulthood: Clues to Diagnosis from Facial Dysmorphism.
    Batra N; Kant R; Mandal K; Joshi K
    Neurol India; 2021; 69(1):161-163. PubMed ID: 33642291
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.
    Liu AP; Chow PC; Lee PP; Mok GT; Tang WF; Lau ET; Lam ST; Chan KY; Kan AS; Chau AK; Cheung YF; Lau YL; Chung BH
    Eur J Med Genet; 2014; 57(6):306-11. PubMed ID: 24721633
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Parkinson's disease with hypocalcaemia: adult presentation of 22q11.2 deletion syndrome.
    Moreira F; Brás A; Lopes JR; Januário C
    BMJ Case Rep; 2018 Mar; 2018():. PubMed ID: 29572372
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.
    Wither RG; Borlot F; MacDonald A; Butcher NJ; Chow EWC; Bassett AS; Andrade DM
    Epilepsia; 2017 Jun; 58(6):1095-1101. PubMed ID: 28448680
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].
    Demily C; Rossi M; Schneider M; Edery P; Leleu A; d'Amato T; Franck N; Eliez S
    Encephale; 2015 Jun; 41(3):266-73. PubMed ID: 25523123
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An Endocrinological Perspective on 22q11.2 Deletion Syndrome: A Single-center Experience.
    Denkboy Öngen Y; Özemri Sağ Ş; Temel ŞG; Eren E
    J Clin Res Pediatr Endocrinol; 2023 Aug; 15(3):285-292. PubMed ID: 37074225
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of hypocalcemia with congenital heart disease in 22q11.2 deletion syndrome.
    Rayannavar A; Levitt Katz LE; Crowley TB; Lessig M; Grand K; Goldmuntz E; Zackai EH; McDonald-McGinn DM
    Am J Med Genet A; 2018 Oct; 176(10):2099-2103. PubMed ID: 30277015
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis].
    Ingrao T; Lambert L; Valduga M; Bosser G; Albuisson E; Leheup B
    Arch Pediatr; 2017 Nov; 24(11):1067-1075. PubMed ID: 28967605
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypocalcaemia in an adult: the importance of not overlooking the cause.
    Abrantes C; Brigas D; Casimiro HJ; Madeira M
    BMJ Case Rep; 2018 Apr; 2018():. PubMed ID: 29622714
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Late maternal diagnosis of DiGeorge syndrome with congenital hypoparathyroidism following antenatal detection of the same 22q11.2 microdeletion syndrome in the fetus.
    Liarakos AL; Tran P; Rao R; Murthy N
    BMJ Case Rep; 2022 May; 15(5):. PubMed ID: 35606033
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An adult case of 22q11.2 deletion syndrome diagnosed in a 36-year-old woman with hypocalcemia caused by hypoparathyroidism and Hashimoto's thyroiditis.
    Nakada Y; Terui K; Kageyama K; Tsushima Y; Murakami H; Soma Y; Nigawara T; Sakihara S
    Intern Med; 2013; 52(12):1365-8. PubMed ID: 23774548
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Delayed diagnosis of 22q11.2 deletion syndrome in an adult Chinese lady.
    Shea YF; Lee CH; Gill H; Chow WS; Lam YM; Luk HM; Lam ST; Chu LW
    Chin Med J (Engl); 2012 Aug; 125(16):2945-7. PubMed ID: 22932096
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.
    Lin HY; Tsai WY; Tung YC; Liu SY; Lee NC; Chien YH; Hwu WL; Lee CT
    Front Endocrinol (Lausanne); 2022; 13():771100. PubMed ID: 35432203
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency.
    Barry JC; Crowley TB; Jyonouchi S; Heimall J; Zackai EH; Sullivan KE; McDonald-McGinn DM
    J Clin Immunol; 2017 Jul; 37(5):476-485. PubMed ID: 28540525
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypocalcemic seizure mistaken for idiopathic epilepsy in two cases of DiGeorge syndrome (chromosome 22q11 deletion syndrome).
    Tsai PL; Lian LM; Chen WH
    Acta Neurol Taiwan; 2009 Dec; 18(4):272-5. PubMed ID: 20329596
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Noncardiac DiGeorge syndrome diagnosed with multiplex ligation-dependent probe amplification: A case report.
    Fu CH; Leung C; Kao CH; Yeh SJ
    J Formos Med Assoc; 2015 Aug; 114(8):769-73. PubMed ID: 26254176
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [DiGeorge syndrome diagnosed in a 39-year old woman with chronic hypocalcemia].
    Hoffmann MH; Vadstrup S
    Ugeskr Laeger; 2000 May; 162(19):2755-6. PubMed ID: 10827545
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 22q11.2 deletion presenting with severe hypocalcaemia, seizure and basal ganglia calcification in an adult man.
    Cao Z; Yu R; Dun K; Burke J; Caplin N; Greenaway T
    Intern Med J; 2011 Jan; 41(1a):63-6. PubMed ID: 21265963
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dental management of a patient with 22q11.2 deletion syndrome (22q11.2DS).
    AlQarni MA; Alharbi A; Merdad L
    BMJ Case Rep; 2018 Sep; 2018():. PubMed ID: 30232069
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.