نتائج البحث

Optic pathway glioma and the sex association in neurofibromatosis type 1: a single-center study

• Authors : Anne Munk Henning; Mette Møller Handrup; Sia Mariann Kjeldsen

Subjects: Neurofibromatosis type 1; Optic pathway glioma; Sex characteristics

• Source: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-7 (2021)

تفاصيل العنوان

Gender differences in hereditary hemorrhagic telangiectasia severity.

• Authors : Mora-Luján JM; HHT Unit, Hospital Universitari de Bellvitge, C/Feixa Llarga s/n. L'Hospitalet de Llobregat, 08907, Barcelona, Spain.; Internal Medicine Department, Hospital Universitari Bellvitge, Barcelona, Spain.

Subjects: Arteriovenous Malformations* ; Liver Diseases* ; Telangiectasia, Hereditary Hemorrhagic*

• Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2020 Mar 02; Vol. 15 (1), pp. 63. Date of Electronic Publication: 2020 Mar 02.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

تفاصيل العنوان

Optic pathway glioma and the sex association in neurofibromatosis type 1: a single-center study.

• Authors : Henning, Anne Munk¹ (AUTHOR) ; Handrup, Mette Møller¹ (AUTHOR); Kjeldsen, Sia Mariann² (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 11/22/2021, Vol. 16 Issue 1, p1-7. 7p.

تفاصيل العنوان

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update.

• Authors : Herlin, Morten Krogh^1,2 (AUTHOR) ; Petersen, Michael Bjørn^1,3 (AUTHOR); Brännström, Mats⁴ (AUTHOR)

• Source: Orphanet Journal of Rare Diseases. 8/20/2020, Vol. 15 Issue 1, pN.PAG-N.PAG. 1p.

تفاصيل العنوان

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update

• Authors : Morten Krogh Herlin; Michael Bjørn Petersen; Mats Brännström

Subjects: MRKH syndrome; MRKHS; Disorders of sex development

• Source: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-16 (2020)

تفاصيل العنوان