Results 61 to 70 of about 34,092 (295)

Familial Frontal Fibrosing Alopecia Occurs Early in Daughters With Affected Mothers: A Case Report and a Review of the Literature

Australasian Journal of Dermatology, EarlyView.
ABSTRACT Frontal fibrosing alopecia (FFA) is a form of cicatricial alopecia that is being increasingly diagnosed in recent years. It predominantly affects post‐menopausal women of various ethnic backgrounds, but cases have also been reported in pre‐menopausal women and rarely in men.
Adrienne Oxenham, Annabel Stevenson
wiley   +1 more source

Influence of Dysmenorrhea and Menorrhagia on Academic Performance among Female Students in Tertiary Institutions in Ondo State Nigeria

, 2016
Objective: The study examined the influence of dysmenorrhea and menorrhagia on academic performance amongtertiary institution female students in Ondo State, Nigeria.Methods: A total of 150 female respondents were selected using purposive sampling ...
C. F. Akinnubi
semanticscholar   +1 more source

Combined factor VIII and IX deficiency: role in puberty menorrhagia: a case report [PDF]

, 2016
The prevalence of menorrhagia in adolescent populations with bleeding disorders varies between 14% to 48%. Hereditary bleeding disorders are an important cause of puberty menorrhagia and the consequences can be life threatening.
Pandey, Vivek Kumar, Sinha, Hemali Heidi, Tiwary, Bhawana   +2 more
core   +2 more sources

Is adenomyosis associated with menorrhagia?

Human Reproduction, 2014
STUDY QUESTION Is the presence of adenomyosis associated with menorrhagia? SUMMARY ANSWER There was no significant association between adenomyosis and menorrhagia, but there was a significant positive correlation between the severity of adenomyosis on ...
J. Naftalin, W. Hoo, K. Pateman, D. Mavrelos, X. Foo, D. Jurković   +5 more
semanticscholar   +1 more source

Identification of 22 novel mutations in patients with Glanzmann's thrombasthenia [PDF]

, 2008
Glanzmann's thrombasthenia (GT) is an autosomal recessive inherited platelet function defect that characterized by reduction in, or absence of, platelet aggregation in response to multiple physiologic agonists. GT is characterized by normal platelet
Abdul Ethayathulla, Birendra Yadav, Firdos Ahmad, Meganathan Kannan, Rajive Kumar, Renu Saxena, Ved Choudhry   +6 more
core   +1 more source

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies [PDF]

, 2016
A paucity of data exists on the incidence, diagnosis and treatment of bleeding in women with inherited factor VII (FVII ...
Batorova, Baumann Kreuziger, Bernardi, Byams, Di Minno, Fasouliotis, Foster, Grant, James, James, Kadir, Kadir, Kadir, Kirtava, Kitchens, Kouides, Kouides, Kulkarni, Kulkarni, Lobo, Lobo, Mariani, Mariani, Mariani, Mariani, Mariani, Napolitano, Napolitano, Peyvandi, Shankar, Warner, Warner, Wellington   +32 more
core   +2 more sources

Ulipristal acetate for Japanese women with symptomatic uterine fibroids: A double‐blind, randomized, phase II dose‐finding study

Reproductive Medicine and Biology, 2020
Purpose A multicenter, randomized, double‐blind, placebo‐controlled trial was conducted to evaluate the efficacy, safety, and appropriate dose of ulipristal acetate (UPA) in Japanese women with symptomatic uterine fibroids (UFs).
Minoru Irahara, Yasuhiro Maejima, Nobuhiro Shinbo, Yuji Yamauchi, Hideki Mizunuma   +4 more
doaj   +1 more source

Quality of life 1 year after uterine artery embolization vs hysterectomy for symptomatic adenomyosis (QUESTA study)

Acta Obstetricia et Gynecologica Scandinavica, EarlyView.
After 1 year, both uterine artery embolization (UAE) and hysterectomy significantly improved health‐related quality of life (HRQOL) for patients with symptomatic adenomyosis. Neither non‐inferiority nor inferiority could be established within the predefined margins. HRQOL after 1 year was comparable in all HRQOL domains after UAE vs. hysterectomy. Both
Lisa M. Trommelen, Annika Semmler, Annefleur M. de Bruijn, Marissa Harmsen, Marieke Smink, Petra F. Janssen, Ilse van Rooij, Jeroen van Bavel, Peggy Geomini, Jacques W. M. Maas, Celine M. Radder, Paul van Kesteren, Janet Kwee, Erica Bakkum, Marleen de Lange, Robert A. de Leeuw, Freek Groenman, Velja Mijatovic, Anne Timmermans, Rutger Lely, Armand Lamers, Douwe Vos, Gretel van Hoecke, Otto Elgersma, Huib A. A. M. van Vliet, Lonneke S. F. Yo, Andries R. H. Twijnstra, Frank W. Jansen, Catharina S. P. van Rijswijk, Han Kruimer, Carroll M. E. S. N. Tseng, Sjors Coppus, Mark Arntz, Aloys F. J. Wust, Joost G. A. M. Blomjous, Laurens van Boven, Alexander Venmans, Jos W. R. Twisk, Judith A. F. Huirne, Paul N. M. Lohle, Wouter J. K. Hehenkamp   +40 more
wiley   +1 more source

Pubertal Menorrhagia: Evaluation and Management

Journal of clinical and biomedical sciences, 2015
OBJECTIVES: To determine the causes of puberty menorrhagia and to evaluate the efficacy of medical management. MATERIALS AND METHODS: This is a prospective observational study included 48 patients who presented with menorrhagic cycles in the pubertal age
A. Sri, A. Jehan
semanticscholar   +1 more source

Clinical Features and Types of Von Willebrand Disease in Women with Menorrhagia Referred to Hematology Clinic of Kermanshah

International Journal of Hematology-Oncology and Stem Cell Research, 2013
Menorrhagia is the most common symptom that is experienced by women with bleeding disorders. Von Willebrand disease (VWD) is the most common congenital human bleeding disorder that is manifested as a quantitative deficiency in Von Willebrand factor (VWF)
Mehrdad Payandeh, Zohreh Rahimi, Atefeh Nasir Kansestani, Shahrooz Hemmati, Mahnaz Aleyasin, Mohammad Erfan Zare, Zohreh Nouri, Amir Hossein Hashemian, Farzad gohardehi   +8 more
doaj   +2 more sources