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Journal Abstract Search

160 related items for PubMed ID: 36120216

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  • 2. Hyaline Fibromatosis Syndrome: A Rare Inherited Disorder.
    Mantri MD, Pradeep MM, Kalpesh PO, Pranavsinh RJ.
    Indian J Dermatol; 2016; 61(5):580. PubMed ID: 27688461
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  • 5. Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report.
    Jaouad IC, Guaoua S, Hajjioui A, Sefiani A.
    J Med Case Rep; 2014 Sep 03; 8():291. PubMed ID: 25186005
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  • 7. Hyaline Fibromatosis Syndrome Presenting with Nasal Mass: A Case Report.
    Alkholaiwi F, Alsheikh A.
    Ear Nose Throat J; 2022 Oct 11; ():1455613221129446. PubMed ID: 36219393
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  • 10. Juvenile non-hyaline fibromatosis: juvenile hyaline fibromatosis without prominent hyaline changes.
    Anadolu RY, Oskay T, Ozsoy N, Erdem C.
    J Cutan Pathol; 2005 Mar 11; 32(3):235-9. PubMed ID: 15701086
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  • 14. A Severe Case of Infantile Systemic Hyalinosis in an Asian Child: A Product of Consanguinity.
    Baroud S, Alawadhi A.
    Cureus; 2021 Jul 11; 13(7):e16433. PubMed ID: 34414050
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  • 15. Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis-A Case Report.
    Krasuska-Sławińska E, Polnik D, Rokicki D, Koeber B.
    J Oral Maxillofac Surg; 2015 Oct 11; 73(10):1962.e1-5. PubMed ID: 26207694
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  • 17. Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review.
    Zhu Y, Du X, Sun L, Wang H, Wang D, Wu B.
    Mol Genet Genomic Med; 2022 Aug 11; 10(8):e1993. PubMed ID: 35726349
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