Mayer-Rokitansky-Küster-Hauser syndrome: distinction between two forms based on excretory urographic, sonographic, and laparoscopic findings.
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Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeThe Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approachesMURCS association: case report and reviewChronic kidney disease in Mayer-Rokitansky-Kuster-Hauser SyndromeUtero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association).Mayer-rokitansky-kuster-hauser syndrome: surgical management of two cases.High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasiaMalformations in a cohort of 284 women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH).A rare case of Mayer-Rokitansky-Kuster-Hauser syndrome with multiple leiomyomas in hypoplastic uterus.Mayer-rokitansky-kuster-hauser syndrome: embryology, genetics and clinical and surgical treatment.Large leiomyoma in a woman with Mayer-Rokitansky-Kuster-Hauser syndrome.A successful laparoscopic neovaginoplasty using peritoneum in Müllerian agenesis with inguinal ovaries accompanied by primary ovarian insufficiencyAre children with congenital solitary kidney at risk for lifelong complications? A lack of prediction demands caution.Retrovesical cystic lesions in female patients with unilateral renal agenesis or dysplasia.The presentation and management of complex female genital malformations.Surrogate in vitro fertilization outcome in typical and atypical forms of Mayer-Rokitansky-Kuster-Hauser syndrome.Hyperandrogenemia and ovarian reserve in patients with Mayer-Rokitansky-Küster-Hauser syndrome type 1 and 2: potential influences on ovarian stimulation.The congenital and acquired solitary kidney.Coexistence of Mayer-Rokitansky-Kuster-Hauser syndrome and neurofibromatosis type I.Total vaginal reconstruction with combined 'Split Labia Minora Flaps' and full-thickness skin grafts.Familial occurrence of Mayer-Rokitansky-Küster-Hauser syndrome: a case report and review of the literature.Exclusion ofWNT4 as a major gene in Rokitansky-Küster-Hauser anomaly
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P2860
Mayer-Rokitansky-Küster-Hauser syndrome: distinction between two forms based on excretory urographic, sonographic, and laparoscopic findings.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh-hant
name
Mayer-Rokitansky-Küster-Hauser ...... ic, and laparoscopic findings.
@en
Mayer-Rokitansky-Küster-Hauser ...... ic, and laparoscopic findings.
@nl
type
label
Mayer-Rokitansky-Küster-Hauser ...... ic, and laparoscopic findings.
@en
Mayer-Rokitansky-Küster-Hauser ...... ic, and laparoscopic findings.
@nl
prefLabel
Mayer-Rokitansky-Küster-Hauser ...... ic, and laparoscopic findings.
@en
Mayer-Rokitansky-Küster-Hauser ...... ic, and laparoscopic findings.
@nl
P2093
P1476
Mayer-Rokitansky-Küster-Hauser ...... ic, and laparoscopic findings.
@en
P2093
Lemmens JA
Strübbe EH
Willemsen WN
P304
P356
10.2214/AJR.160.2.8424345
P407
P577
1993-02-01T00:00:00Z