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 *

128 related articles for article (PubMed ID: 13423945)

  • 1. Ocular metastases in Hutchison-Pepper syndrome.
    DAS GUPTA BK; ROY S
    AMA Arch Ophthalmol; 1957 Jun; 57(6):821-31. PubMed ID: 13423945
    [No Abstract]   [Full Text] [Related]  

  • 2. [Sympathoma with hepatic symptomatology (Pepper's syndrome) in a 45 day old infant].
    GIRAUD P; BERNARD R; VINCENT P; GAUJOUX
    Arch Fr Pediatr; 1954; 11(7):758-63. PubMed ID: 13218756
    [No Abstract]   [Full Text] [Related]  

  • 3. [On a very unusual case of association of Pepper's syndrome with an idiopathic true precocious puberty syndrome].
    ROSSI GB; LAGONIGRO F; GALLORO V
    Riv Anat Patol Oncol; 1960 Nov; 18():623-57. PubMed ID: 14494271
    [No Abstract]   [Full Text] [Related]  

  • 4. Early ocular findings in Cohen syndrome: case report and Canadian survey study.
    Quinn MP; MacKeen LD; Vincent A; Strube YNJ
    Can J Ophthalmol; 2021 Feb; 56(1):e26-e28. PubMed ID: 32777201
    [No Abstract]   [Full Text] [Related]  

  • 5. Neonatal neuroblastoma 4s with diffuse liver metastases (Pepper syndrome) without an adrenal/extraadrenal primary identified on imaging.
    Chaturvedi A; Katzman PJ; Franco A
    J Radiol Case Rep; 2018 Mar; 12(3):18-27. PubMed ID: 29875990
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital neuroblastoma: an autopsy report.
    Gupta K; Bansal A
    Fetal Pediatr Pathol; 2012 Oct; 31(5):331-5. PubMed ID: 22432426
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bilateral angle closure glaucoma in a 28-year-old Cohen syndrome patient.
    Li A; Gandhi A; Wang H; Traboulsi EI
    Ophthalmic Genet; 2018 Oct; 39(5):657-658. PubMed ID: 29985682
    [No Abstract]   [Full Text] [Related]  

  • 8. [Use of biotherapy for psoriasis in a patient with Cohen syndrome].
    Fougerousse AC
    Ann Dermatol Venereol; 2020 Dec; 147(12):880-881. PubMed ID: 32747030
    [No Abstract]   [Full Text] [Related]  

  • 9. Nonleaking cystoid macular edema in Cohen syndrome.
    Beck KD; Wong RW; Gibson JB; Harper CA
    J AAPOS; 2019 Feb; 23(1):38-39.e1. PubMed ID: 30144585
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Optical coherence tomography findings in Cohen syndrome.
    Huang LC; Kelly JP; Cabrera MT; Olmos de Koo LC; Weiss AH; Herlihy EP
    J AAPOS; 2020 Oct; 24(5):306-309. PubMed ID: 32919079
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neuroblastoma of the adrenal with orbital metastases; report of five cases with autopsy findings.
    SHAFFER RN
    Am J Ophthalmol; 1947 Jun; 30(6):733-40. PubMed ID: 20241738
    [No Abstract]   [Full Text] [Related]  

  • 12. Cerebellar hypoplasia and Cohen syndrome: a confirmed association.
    Waite A; Somer M; O'Driscoll M; Millen K; Manson FD; Chandler KE
    Am J Med Genet A; 2010 Sep; 152A(9):2390-3. PubMed ID: 20683995
    [No Abstract]   [Full Text] [Related]  

  • 13. [Adrenal neuroblastoma with peri-orbital metastasis].
    PEREZ STABLE M; GUERNICA A
    Rev Cubana Pediatr; 1962; 24():15-20. PubMed ID: 14485315
    [No Abstract]   [Full Text] [Related]  

  • 14. [Seven cases of Stein-Leventhal-Cohen syndrome].
    SCHOCKAERT JA
    C R Soc Fr Gyncol; 1955 Dec; 25(8):402-9. PubMed ID: 13317370
    [No Abstract]   [Full Text] [Related]  

  • 15. Gene analysis: A rare gene disease of intellectual deficiency-Cohen syndrome.
    Yang C; Hou M; Li Y; Sun D; Guo Y; Liu P; Liu Y; Song J; Zhang N; Wei W; Chen Z
    Int J Dev Neurosci; 2018 Aug; 68():83-88. PubMed ID: 29758347
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel VPS13B mutation in Cohen syndrome: a case report and review of literature.
    Momtazmanesh S; Rayzan E; Shahkarami S; Rohlfs M; Klein C; Rezaei N
    BMC Med Genet; 2020 Jun; 21(1):140. PubMed ID: 32605629
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Case report: two novel VPS13B mutations in a Chinese family with Cohen syndrome and hyperlinear palms.
    Zhao S; Luo Z; Xiao Z; Li L; Zhao R; Yang Y; Zhong Y
    BMC Med Genet; 2019 Nov; 20(1):187. PubMed ID: 31752730
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cohen syndrome combined with psychiatric symptoms: a case report.
    Li X; Qi S; Li W; Liu X; Xue Z; Yu T; Xun G
    BMC Psychiatry; 2024 Mar; 24(1):180. PubMed ID: 38439002
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Value of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patients.
    Prokudin I; Li D; He S; Guo Y; Goodwin L; Wilson M; Rose L; Tian L; Chen Y; Liang J; Keating B; Xu X; Jamieson RV; Hakonarson H
    Clin Exp Ophthalmol; 2015 Mar; 43(2):132-8. PubMed ID: 25060287
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Early photoreceptor outer segment loss and retinoschisis in Cohen syndrome.
    Uyhazi KE; Binenbaum G; Carducci N; Zackai EH; Aleman TS
    Ophthalmic Genet; 2018 Jun; 39(3):399-404. PubMed ID: 29634382
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.