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 *

140 related articles for article (PubMed ID: 35651450)

  • 1. Primary Hypoparathyroidism Presenting as Idiopathic Intracranial Hypertension in a Patient With Barakat Syndrome.
    Alkaissi HR; Banerji MA
    Cureus; 2022 Apr; 14(4):e24521. PubMed ID: 35651450
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Syndrome Presenting With Febrile Seizures and Hypocalcemia.
    Gandolfi A; Ratnasamy K; Minutti C
    JCEM Case Rep; 2023 Jan; 1(1):luac025. PubMed ID: 37908274
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Concomitant hypoparathyroidism, sensorineural deafness, and renal agenesis: a case of Barakat syndrome.
    Ranjbar-Omrani G; Zamiri N; Sabayan B; Mohammadzadeh A
    Arch Iran Med; 2008 May; 11(3):337-40. PubMed ID: 18426329
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Barakat syndrome].
    Berkešová BA; Borbély Z
    Vnitr Lek; 2023; 69(E-3):16-19. PubMed ID: 37468331
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Benign Intracranial Hypertension Due to Hypoparathyroidism: A Case Report.
    Sforza G; Deodati A; Moavero R; Papetti L; Frattale I; Vigevano F; Cianfarani S; Valeriani M
    Front Neurol; 2021; 12():818638. PubMed ID: 35082750
    [No Abstract]   [Full Text] [Related]  

  • 6. Seizure, deafness, and renal failure: a case of barakat syndrome.
    Maleki N; Bashardoust B; Iranparvar Alamdari M; Tavosi Z
    Case Rep Nephrol; 2013; 2013():261907. PubMed ID: 24527244
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Seizure, deafness and renal agenesis: A rare case of barakat syndrome.
    Sau T; Chatterjee A; Ghosh K; Dey S
    Ann Indian Acad Neurol; 2013 Jan; 16(1):91-3. PubMed ID: 23661972
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3: a case report and review of literature.
    Joseph ADD; Sirisena ND; Kumanan T; Sujanitha V; Strelow V; Yamamoto R; Wieczorek S; Dissanayake VHW
    BMC Endocr Disord; 2019 Oct; 19(1):111. PubMed ID: 31660939
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial congenital choanal atresia with GATA3 associated hypoparathyroidism-deafness-renal dysplasia syndrome unidentified on auditory brainstem response.
    Kita M; Kuwata Y; Usui T
    Auris Nasus Larynx; 2019 Oct; 46(5):808-812. PubMed ID: 30396722
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial idiopathic hypoparathyroidism, sensorineural deafness and renal dysplasia.
    Ishida S; Isotani H; Kameoka K; Kishi T
    Intern Med; 2001 Feb; 40(2):110-3. PubMed ID: 11300141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. HDR syndrome with a novel mutation in GATA3 mimicking a congenital X-linked stapes gusher: a case report.
    Yang A; Kim J; Ki CS; Hong SH; Cho SY; Jin DK
    BMC Med Genet; 2017 Oct; 18(1):121. PubMed ID: 29073906
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Idiopathic hypoparathyroidism with extensive intracranial calcification in children: First report from Saudi Arabia.
    Kamal NM; Alghamdi HA; Halabi AA; Bakkar AA; Algarni A; Alharbi A; Alharthi AA; Alharbi RA; Sherief LM
    Medicine (Baltimore); 2017 Apr; 96(16):e6347. PubMed ID: 28422826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Treatment of severe life threatening hypocalcemia with recombinant human teriparatide in patients with postoperative hypoparathyroidism - a case series.
    Andrysiak-Mamos E; Żochowska E; Kaźmierczyk-Puchalska A; Popow M; Kaczmarska-Turek D; Pachucki J; Bednarczuk T; Syrenicz A
    Endokrynol Pol; 2016; 67(4):403-12. PubMed ID: 27387245
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Medical Hypoparathyroidism.
    Siraj N; Hakami Y; Khan A
    Endocrinol Metab Clin North Am; 2018 Dec; 47(4):797-808. PubMed ID: 30390814
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hypoparathyroidism.
    Hakami Y; Khan A
    Front Horm Res; 2019; 51():109-126. PubMed ID: 30641528
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Causes and differential diagnosis of hypocalcemia--recommendation proposed by expert panel supported by ministry of health, labour and welfare, Japan.
    Fukumoto S; Namba N; Ozono K; Yamauchi M; Sugimoto T; Michigami T; Tanaka H; Inoue D; Minagawa M; Endo I; Matsumoto T
    Endocr J; 2008 Oct; 55(5):787-94. PubMed ID: 18490837
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Primary Hypoparathyroidism Mimicking Ankylosing Spondylitis in a Young Man with Fahr's Syndrome: A Case Report.
    Sasi S; Rahil A; Vattoth S; Cackamvalli P; Abdullah W
    Cureus; 2020 Sep; 12(9):e10426. PubMed ID: 32944487
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Normocalcemic hyperparathyroidism and hypoparathyroidism in two community-based nonreferral populations.
    Cusano NE; Maalouf NM; Wang PY; Zhang C; Cremers SC; Haney EM; Bauer DC; Orwoll ES; Bilezikian JP
    J Clin Endocrinol Metab; 2013 Jul; 98(7):2734-41. PubMed ID: 23690312
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Barakat syndrome revisited.
    Barakat AJ; Raygada M; Rennert OM
    Am J Med Genet A; 2018 Jun; 176(6):1341-1348. PubMed ID: 29663634
    [TBL] [Abstract][Full Text] [Related]  

  • 20. HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome presenting with hypocalcemia-induced generalized psoriasis.
    Aksoylar S; Aydinok Y; Serdaroğlu E; Coker M; Ozdemir F; Ozkinay F
    J Pediatr Endocrinol Metab; 2004 Jul; 17(7):1031-4. PubMed ID: 15301053
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.