Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging. - Wikidata - wikimedia - TriplyDB

Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging.

Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging.

http://www.wikidata.org/entity/Q33991395

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Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome Mayer-Rokitansky-Kuster-Hauser syndrome: a review Experimental uterus transplantation Mayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findings An update on surgical and non-surgical treatments for vaginal hypoplasia.Information ranks highest: Expectations of female adolescents with a rare genital malformation towards health care services.Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report.Mayer-rokitansky-kuster-hauser syndrome associated with severe inferior vena cava stenosis.Molecular genetics of Müllerian duct formation, regression and differentiation Development of a provisional model to improve transitional care for female adolescents with a rare genital malformation as an example for orphan diseases.Endometriosis in a patient with mayer-rokitansky-küster-hauser syndrome Importance of Laparoscopic Assessment of the Uterine Adnexa in a Mayer-Rokitansky-Kuster-Hauser Syndrome Type II Case.A case of swyer syndrome associated with advanced gonadal dysgerminoma involving long survival.High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia Clinical approach for the classification of congenital uterine malformations Mayer-Rokitansky-Kuster-Hauser syndrome diagnosed by magnetic resonance imaging. Role of imaging to identify and evaluate the uncommon variation in development of the female genital tract Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature Malformations in a cohort of 284 women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH).Personality traits and coping styles in women with Mayer-Rokitansky-Küster-Hauser syndrome.Leiomyoma Arising from Mullerian Remnant, Mimicking Ovarian Tumor in a Woman with MRKH Syndrome and Unilateral Renal Agenesis.Mayer-rokitansky-kuster-hauser syndrome: embryology, genetics and clinical and surgical treatment.MURCS Association with Partial Duplication of the Distal Long Chromosome 5 and Unilateral Ovarian Agenesis.Molecular analysis of the beta-catenin gene in patients with the Mayer-Rokitansky-Küster-Hauser syndrome.A successful laparoscopic neovaginoplasty using peritoneum in Müllerian agenesis with inguinal ovaries accompanied by primary ovarian insufficiency A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3.Multicentric paraspinal neuroglial heterotopia with Müllerian and renal agenesis: a variant of Mayer-Rokitansky-Küster-Hauser syndrome?Pulmonary aplasia with unusual associations in a woman.Risks for donors in uterus transplantation.A systematic approach to the magnetic resonance imaging-based differential diagnosis of congenital Müllerian duct anomalies and their mimics.Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation.The presentation and management of complex female genital malformations.Human uterus transplantation in focus.Prevalence and patient characteristics of Mayer-Rokitansky-Küster-Hauser syndrome: a nationwide registry-based study.Disorders of sex development (DSD): not only babies with ambiguous genitalia. A practical guide for surgeons.Mullerian dysgenesis: a critical review of the literature.Should human beings have sex? Sexual dimorphism and human enhancement.Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.Surrogate in vitro fertilization outcome in typical and atypical forms of Mayer-Rokitansky-Kuster-Hauser syndrome.Uterus transplantation: Toward clinical application in Japan.Congenital Malformations of the Reproductive Tract in a Patient with Poland Syndrome: Is There a Connection?

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P2860

Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging.

http://www.wikidata.org/entity/Q33991395

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2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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Clinical aspects of Mayer-Roki ...... linical diagnosis and staging.

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Clinical aspects of Mayer-Roki ...... linical diagnosis and staging.

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Clinical aspects of Mayer-Roki ...... linical diagnosis and staging.

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Clinical aspects of Mayer-Roki ...... linical diagnosis and staging.

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Human Reproduction

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Clinical aspects of Mayer-Roki ...... linical diagnosis and staging.

@en

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Anja Kellermann

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Georges A Hauser

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Kurt S Ludwig

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Pamela L Strissel

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Peter Oppelt

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Reiner Strick

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Sara Brucker

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Stefan P Renner

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P2860

The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia.

Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome.

Spinal abnormalities and the atypical form of the Mayer-Rokitansky-Küster-Hauser syndrome.

Anatomic and functional results of laparoscopic-perineal neovagina construction by sigmoid colpoplasty in women with Rokitansky's syndrome.

Bilateral ovarian agenesis and the presence of the testis-specific protein 1-Y-linked gene: two new features of Mayer-Rokitansky-Küster-Hauser syndrome.

Further evidence that the WT1 gene does not have a role in the development of the derivatives of the müllerian duct.

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792-797

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scholarly article

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10.1093/HUMREP/DEI381

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3

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21

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Diethelm Wallwiener

Matthias W. Beckmann

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2005-11-10T00:00:00Z

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7484474

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16284062

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