نتایج جستجو برای: mullerian hormon

تعداد نتایج: 2883  

2013
M. Dólleman M. J. Faddy J. van Disseldorp Y. T. van der Schouw C. M. Messow B. Leader P. H. M. Peeters A. McConnachie S. M. Nelson F. J. M. Broekmans

(2013) The relationship between anti-mullerian hormone in women receiving fertility assessments and age at menopause in subfertile women: evidence from large population studies. The content must not be changed in any way or reproduced in any format or medium without the formal permission of the copyright holder(s) When referring to this work, full bibliographic details must be given

2013
Kai J. Buhling Petra Stute Volker Ziller

Anti-Mullerian hormone (AMH) is a protein that inhibits the development of the mullerian ducts (paramesonephric ducts) in the male embryo. AMH prevents the development of the mullerian ducts into the uterus and other mullerian structures in the first 8 weeks of gestational age. AMH is produced by granulosa cells of the ovary during the reproductive years and controls the formation of primary fo...

Journal: :Reproductive biology 2013
Emily Zuvela Melanie Walls Phillip Matson

Ten laboratories in an external quality assurance scheme used the same assay to measure anti-müllerian hormone concentration (Beckman Coulter Gen II) and received twenty serum samples distributed over a 15 month period. The mean bias for all results was only -0.089%, but there was large coefficient of repeatability of 38.8% (sample bias ranged from -37.9% to +54.7%). While each laboratory showe...

Journal: :Journal of the Turkish German Gynecological Association 2011
Ibrahim Hakan Boyar Fazilet Kübra Boynukalın Nuray Boyar Mehmet Vural

Congenital anomalies of the uterus may cause gynecologic, obstetric and fertility problems. Obstetrical complications are reported to occur more commonly with mullerian duct anomalies, such as postpartum hemorrhage (PPH). Uterine compression sutures may be effective in controlling PPH in these conditions as an alternative to hysterectomy, especially if the patient has a desire to conceive. As t...

اکبری اسبق, فیروزه , خادمی, افسانه ,

Mullerian anomalies are one of the interesting but uncommon entities that gynecologists confront. The incidence is 1-6%, It is difficult to" anticipate the real incidence, because most of information is obtained from infertile or complicated patients with inadequate work-up. Recently endoscopic pocedures reveal more details about these anomalies. Today, classification of Buttram & Gibbons (modi...

2013
Tsuyoshi Shinohara Hiroyuki Yamada Yoshiro Fujimori Kiyofumi Yamagishi

Patient: Female, 94 Final Diagnosis: Malignant pleural effusion Symptoms: - Medication: - Clinical Procedure: Cytology Specialty: Oncology. OBJECTIVE Unusual clinical course. BACKGROUND The most common site of postoperative breast cancer recurrence is bone, followed by local relapse, lung, and liv...

2015
Müberra Namlı Kalem Ziya Kalem Ebru Yüce Ayla Eser Zehra Candan İltemir Duvan

In the last 20 to 30 years, early diagnosis of pregnancy has markedly decreased ectopic pregnancy-related maternal mortality, and the necessity for surgical treatment. With modern approaches in the treatment of ectopic pregnancy, surgical therapy has been replaced by medical therapy and medical treatment by spontaneous follow-up in appropriate cases. However, this current trend has led to some ...

2011
Muhammad Zafar Iqbal Mazhar Rafee Jam Muhammad Saleem Mushtaq Ahmad

True hermaphrodite is one of the rarest variety of disorders of sexual differentiation (DSD) and represents only 5% cases of all. A 3-year-old child presented with left sided undescended testis and penoscrotal hypospadias. Chordee correction was performed 18 months back, elsewhere. At laparotomy Mullerian structures were present on left side. On right side testis was normally descended into the...

1979
A. E. Duraisamy

Abnormal fusion of the mullerian ducts causes variyng degrees of congenital uterine anomalies, associated with reproductive problems. Twin gestation in a case of bicornuate uterus is extremely rare and with a poor reproductive performance. We are reporting this case because there are only a few cases, less than 20, in previous reports.

Journal: :Journal of medical genetics 1987
T I Farag S A Al-Awadi P Tippett M el-Sayed T S Sundareshan S A Al-Othman M H el-Badramany

A 13 year old female presented with ambiguous external genitalia, right inguinal ovotestis, left ovary, apparently normal Mullerian system, and absent Wolffian system. Cultured lymphocytes showed a 46,XX/46,XY karyotype. Histopathology of the gonads confirmed true hermaphroditism. The presence of two genetically different erythrocyte populations was observed. The findings suggested that the pat...

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