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 *

162 related articles for article (PubMed ID: 15372524)

  • 21. Adams-Oliver Syndrome: A Case with Full Expression.
    Dehdashtian A; Dehdashtian M
    Pediatr Rep; 2016 Jun; 8(2):6517. PubMed ID: 27433307
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Adams-Oliver syndrome and hepatoportal sclerosis: occasional association or common mechanism?
    Girard M; Amiel J; Fabre M; Pariente D; Lyonnet S; Jacquemin E
    Am J Med Genet A; 2005 Jun; 135(2):186-9. PubMed ID: 15832360
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Adams-Oliver syndrome: a case of bilateral progressive ischemic maculopathy.
    Naravane AV; Belin PJ; Bhambhani V; Quiram PA
    J AAPOS; 2020 Jun; 24(3):186-188. PubMed ID: 32522703
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Treatment of a Large Skull Defect and Brain Herniation in a Newborn With Adams-Oliver Syndrome.
    Wehrens KM; De Jongh F; Ter Laak MP; Cornips EM; Van der Hulst R
    Cureus; 2020 Feb; 12(2):e7047. PubMed ID: 32211278
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases.
    Mempel M; Abeck D; Lange I; Strom K; Caliebe A; Beham A; Kautza M; Worret WI; Neubauer BA; Ring J; Schröder H; Fölster-Holst R
    Br J Dermatol; 1999 Jun; 140(6):1157-60. PubMed ID: 10354089
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
    Caksen H; Kurtoğlu S
    Acta Neurol Belg; 2000 Dec; 100(4):252-5. PubMed ID: 11233683
    [TBL] [Abstract][Full Text] [Related]  

  • 27. DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies.
    Sukalo M; Tilsen F; Kayserili H; Müller D; Tüysüz B; Ruddy DM; Wakeling E; Ørstavik KH; Snape KM; Trembath R; De Smedt M; van der Aa N; Skalej M; Mundlos S; Wuyts W; Southgate L; Zenker M
    Hum Mutat; 2015 Jun; 36(6):593-8. PubMed ID: 25824905
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Adams-Oliver syndrome: a case with minimal expression].
    Messerer M; Diabira S; Belliard H; Hamlat A
    Arch Pediatr; 2010 Oct; 17(10):1460-4. PubMed ID: 20728324
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Aplasia cutis congenita, terminal limb defects and falciform retinal folds: confirmation of a distinct syndrome of vascular disruption.
    Prothero J; Nicholl R; Wilson J; Wakeling EL
    Clin Dysmorphol; 2007 Jan; 16(1):39-41. PubMed ID: 17159513
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation.
    Yağci-Küpeli B; Çağlar K; Büyük S; Balci S
    Genet Couns; 2011; 22(1):55-61. PubMed ID: 21614989
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Adams Oliver syndrome: a family with extreme variability in clinical expression.
    Bamforth JS; Kaurah P; Byrne J; Ferreira P
    Am J Med Genet; 1994 Feb; 49(4):393-6. PubMed ID: 8160731
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Adams-Oliver syndrome with widespread CMTC and fatal pulmonary vascular disease.
    Dadzie OE; Tyszczuk L; Holder SE; Teixeira F; Charakida A; Scarisbrick J; Chu A
    Pediatr Dermatol; 2007; 24(6):651-3. PubMed ID: 18035989
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations.
    Jones KM; Silfvast-Kaiser A; Leake DR; Diaz LZ; Levy ML
    Pediatr Dermatol; 2017 Sep; 34(5):e249-e253. PubMed ID: 28884918
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Adams-Oliver syndrome: aplasia cutis congenita, terminal transverse limb defects and cutis marmorata telangiectatica congenita.
    Dyall-Smith D; Ramsden A; Laurie S
    Australas J Dermatol; 1994; 35(1):19-22. PubMed ID: 7998895
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Multifocal aplasia cutis congenita, distal limb hemimelia, and cutis marmorata telangiectatica in a patient with Adams-Oliver syndrome.
    Bork K; Pfeifle J
    Br J Dermatol; 1992 Aug; 127(2):160-3. PubMed ID: 1390145
    [No Abstract]   [Full Text] [Related]  

  • 36. Severe phenotype in two half-sibs with Adams Oliver syndrome.
    Sevilla-Montoya R; Ríos-Flores B; Moreno-Verduzco E; Domínguez-Castro M; Rivera-Pedroza CI; Aguinaga-Ríos DM
    Arch Argent Pediatr; 2014 Jun; 112(3):e108-12. PubMed ID: 24862819
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutations in NOTCH1 cause Adams-Oliver syndrome.
    Stittrich AB; Lehman A; Bodian DL; Ashworth J; Zong Z; Li H; Lam P; Khromykh A; Iyer RK; Vockley JG; Baveja R; Silva ES; Dixon J; Leon EL; Solomon BD; Glusman G; Niederhuber JE; Roach JC; Patel MS
    Am J Hum Genet; 2014 Sep; 95(3):275-84. PubMed ID: 25132448
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn.
    Rojnueangnit K; Phawan T; Khetkham T; Techasatid W; Sirichongkolthong B
    Am J Med Genet A; 2022 Feb; 188(2):658-664. PubMed ID: 34755929
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Transverse limb defects associated with aorto-pulmonary vascular abnormalities: vascular disruption sequence or atypical presentation of Adams-Oliver syndrome?
    Al-Sanna'a N; Adatia I; Teebi AS
    Am J Med Genet; 2000 Oct; 94(5):400-4. PubMed ID: 11050626
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Adams-Oliver syndrome associated with bilateral anterior polar cataracts and optic disk drusen.
    Lascaratos G; Lam WW; Newman WD; MacRae M
    J AAPOS; 2011 Jun; 15(3):299-301. PubMed ID: 21641251
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.