Results 71 to 80 of about 9,042 (179)

Robot-assisted hysterectomy in a 41-year-old male: A rare case report

open access: yesUrology Case Reports, 2020
Persistent Müllerian Duct Syndrome (PMDS) is regarded as a rare genetic disorder influencing internal sexual male development. PMDS is commonly diagnosed incidentally either during any pelvic surgery or examination of undescended testis.
Saud Almousa   +5 more
doaj   +1 more source

Insects and Survival: A Review of Primary and Secondary Defense Strategies

open access: yesEntomologia Experimentalis et Applicata, EarlyView.
Based on a review of three decades of literature, insect defense mechanisms are classified into primary (I) and secondary (II) mechanisms of behavioral, morphological, and chemical nature. These mechanisms have been recorded in 22 (I) and 20 (II) orders, respectively.
Lucas Fernandes Silva   +3 more
wiley   +1 more source

Spreading the clinical window for diagnosing fetal-onset hypogonadism in boys [PDF]

open access: yes, 2014
In early fetal development, the testis secretes – independent of pituitary gonadotropins – androgens and anti-Müllerian hormone (AMH) that are essential for male sex differentiation. In the second half of fetal life, the hypothalamic–pituitary axis gains
Ambao, Veronica Ana   +12 more
core   +2 more sources

A successful in vitro fertilization outcome in a hermaphrodite male

open access: yes
International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 424-425, April 2025.
Shima Elbakhit M. E. Albasha   +2 more
wiley   +1 more source

The junction between the midgut and hindgut co‐localizes with the rectosigmoid junction

open access: yesJournal of Anatomy, EarlyView.
At 5 weeks of development, the midgut has formed its primary loop (left). It is well established that the midgut is bounded cranially by the caudal end of the ventral mesentery and the presence of the common bile duct, but its caudal boundary remains to be established.
Hui Gao   +5 more
wiley   +1 more source

Magnetic resonance imaging in diagnosis and classification of uterovaginal congenital anomalies

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Uterine congenital anomalies are clinically relevant because these are associated with increased incidences of infertility and menstrual disorder. These are frequently not diagnosed at birth.
Pratiksha Yadav
doaj   +1 more source

Müllerian duct anomalies with term pregnancy: a case report

open access: yesJournal of Medical Case Reports, 2020
Background Müllerian duct anomaly is a rare condition. Many cases remain unidentified, especially if asymptomatic. Thus, it is difficult to determine the actual incidence.
Engku Ismail Engku-Husna   +2 more
doaj   +1 more source

Fibroids in obstructed hemivagina and ipsilateral renal anomaly‐like syndrome: Successful hysterectomy and vaginal septoplasty in a kidney transplant recipient with uterus didelphys, vaginal septum and renal agenesis

open access: yes
International Journal of Gynecology &Obstetrics, EarlyView.
Mariana Correia Moreira Cruz   +5 more
wiley   +1 more source

Psychogenic polydipsia in dogs – a review of pathogenesis, diagnosis and treatment

open access: yesJournal of Small Animal Practice, EarlyView.
Polyuria and polydipsia represent a common clinical presentation in dogs and may result from numerous disorders affecting different body systems. Compulsive water consumption is characteristic of psychogenic polydipsia, a primary polydipsia disorder rooted in neurologic, behavioural or environmental factors.
G. Pavlovsky
wiley   +1 more source

Management of Transverse Testicular Ectopia with Persistent Mullerian Duct Syndrome

open access: yesİstanbul Kuzey Klinikleri, 2018
According to additional anomalies, transverse testicular ectopia (TTE) is classified into three groups. Type-2 TTE, accompanied by persistent mullerian duct syndrome, constitutes approximately 20% of the patients.
Sabri Cansaran   +4 more
doaj   +1 more source

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