BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 22764442)

  • 1. Sanjad Sakati syndrome: a case series from Jordan.
    Albaramki J; Akl K; Al-Muhtaseb A; Al-Shboul M; Mahmoud T; El-Khateeb M; Hamamy H
    East Mediterr Health J; 2012 May; 18(5):527-31. PubMed ID: 22764442
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sanjad-Sakati syndrome in a Tunisian child.
    Kerkeni E; Sakka R; Sfar S; Bouaziz S; Ghedira N; Ben Ameur K; Ben Hmida H; Chioukh FZ; Ghédira ES; Gribaa M; Monastiri K
    Arch Pediatr; 2015 Sep; 22(9):951-5. PubMed ID: 26231322
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Additional Tunisian patients with Sanjad-Sakati syndrome: A review toward a consensus on diagnostic criteria.
    Touati A; Nouri S; Halleb Y; Kmiha S; Mathlouthi J; Tej A; Mahdhaoui N; Ben Ahmed A; Saad A; Bensignor C; H'mida Ben Brahim D
    Arch Pediatr; 2019 Feb; 26(2):102-107. PubMed ID: 30638765
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of severe TBCE-negative hypoparathyroidism-retardation-dysmorphism syndrome: Case report and literature review.
    Ryabets-Lienhard A; Issaranggoon Na Ayuthaya S; Graham JM; Pitukcheewanont P
    Am J Med Genet A; 2018 Aug; 176(8):1768-1772. PubMed ID: 30055029
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Bedouin mutation c.155-166del of the TBCE gene in a patient with Sanjad-Sakati syndrome of Moroccan origin.
    Ratbi I; Lyahyai J; Kabiri M; Banouar M; Zerkaoui M; Barkat A; Sefiania A
    Ann Saudi Med; 2015; 35(2):170-2. PubMed ID: 26336027
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad-Sakati syndrome.
    Aminzadeh M; Galehdari H; Shariati G; Malekpour N; Ghandil P
    J Pediatr (Rio J); 2020; 96(1):60-65. PubMed ID: 30080992
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sanjad-Sakati Syndrome: Oral Health Care.
    Hassona Y; Rajab L; Taimeh D; Scully C
    Med Princ Pract; 2018; 27(3):293-296. PubMed ID: 29533933
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sanjad-Sakati syndrome with macrocytic anemia and failure to thrive: a case from South Jordan.
    Ajarmeh SA; Al Tamimi EM
    J Pediatr Endocrinol Metab; 2018 Apr; 31(5):581-584. PubMed ID: 29494340
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Overlapping phenotype comprising Kenny-Caffey type 2 and Sanjad-Sakati syndromes: The first case report.
    Cavole TR; Perrone E; de Faria Soares MF; Dias da Silva MR; Maeda SS; Lazaretti-Castro M; Alvarez Perez AB
    Am J Med Genet A; 2020 Dec; 182(12):3029-3034. PubMed ID: 33010201
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinement.
    Diaz GA; Gelb BD; Ali F; Sakati N; Sanjad S; Meyer BF; Kambouris M
    Am J Med Genet; 1999 Jul; 85(1):48-52. PubMed ID: 10377012
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Status epilepticus in a child with Sanjad Sakati syndrome.
    Prasad R; Kumari C; Mishra OP; Singh UK
    BMJ Case Rep; 2013 Feb; 2013():. PubMed ID: 23378547
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in Kuwait.
    Naguib KK; Gouda SA; Elshafey A; Mohammed F; Bastaki L; Azab AS; Alawadi SA
    East Mediterr Health J; 2009; 15(2):345-52. PubMed ID: 19554981
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital neuroblastoma in a neonate with hypoparathyroidism-retardation-dysmorphism syndrome.
    Golan-Tripto I; Ling E; Hershkovitz E; Fruchtman Y; Hazan G
    Clin Dysmorphol; 2020 Jan; 29(1):46-48. PubMed ID: 31205051
    [No Abstract]   [Full Text] [Related]  

  • 14. Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and review.
    Courtens W; Wuyts W; Poot M; Szuhai K; Wauters J; Reyniers E; Eleveld M; Diaz G; Nöthen MM; Parvari R
    Am J Med Genet A; 2006 Mar; 140(6):611-7. PubMed ID: 16470743
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hypoparathyroidism in children: a study of eight cases.
    Maaloul I; Aloulou H; Kmiha S; Belfitouri Y; Kamoun H; Fakhfakh F; Chabchoub I; Kammoun T; Hachicha M
    Tunis Med; 2018; 96(8-9):472-476. PubMed ID: 30430523
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sanjad Sakati syndrome and sleep-disordered breathing: an undisclosed association.
    Al-Yaarubi S; Al-Abri AS; Al-Kindi H; Al-Abri M; Naz T; Khater D
    Sleep Breath; 2022 Jun; 26(2):815-821. PubMed ID: 34368942
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sanjad-Sakati Syndrome in a 35-day-old Iraqi Infant: A Case Report.
    Al Ajeli MH
    Oman Med J; 2024 Jan; 39(1):e600. PubMed ID: 38433956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.
    Parvari R; Hershkovitz E; Grossman N; Gorodischer R; Loeys B; Zecic A; Mortier G; Gregory S; Sharony R; Kambouris M; Sakati N; Meyer BF; Al Aqeel AI; Al Humaidan AK; Al Zanhrani F; Al Swaid A; Al Othman J; Diaz GA; Weiner R; Khan KT; Gordon R; Gelb BD;
    Nat Genet; 2002 Nov; 32(3):448-52. PubMed ID: 12389028
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Visceral myopathy causing chronic intestinal pseudoobstruction and intestinal failure in a child with Sanjad-Sakati syndrome.
    Pal K; Moammar H; Mitra DK
    J Pediatr Surg; 2010 Feb; 45(2):430-4. PubMed ID: 20152369
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ophthalmic features of hypoparathyroidism-retardation-dysmorphism.
    Khan AO; Al-Assiri A; Al-Mesfer S
    J AAPOS; 2007 Jun; 11(3):288-90. PubMed ID: 17257873
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.