Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 1
1992 2
2000 1
2002 1
2005 1
2006 1
2007 1
2009 1
2010 3
2011 2
2012 4
2013 2
2014 2
2015 2
2018 2
2020 1
2022 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

24 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome"
Page 1
Ciliopathy: Alstrom Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:179-180. doi: 10.1007/978-3-319-95046-4_35. Adv Exp Med Biol. 2018. PMID: 30578508 Review.
Alstrom syndrome is an autosomal recessive disease with multisystem involvement, including cone-rod dystrophy, hearing loss, type 2 diabetes, insulin resistance with hyperinsulinemia, dilated cardiomyopathy, and progressive hepatic and renal failure. ...The fundus s …
Alstrom syndrome is an autosomal recessive disease with multisystem involvement, including cone-rod dystrophy, hearing loss, type 2 d …
Alstrom syndrome.
Marshall JD, Beck S, Maffei P, Naggert JK. Marshall JD, et al. Eur J Hum Genet. 2007 Dec;15(12):1193-202. doi: 10.1038/sj.ejhg.5201933. Epub 2007 Oct 17. Eur J Hum Genet. 2007. PMID: 17940554
Alstrom Syndrome is an autosomal recessive, single gene disorder caused by mutations in ALMS1 (Chr 2p13), a novel gene of currently unknown molecular function. ...Other clinical features in some patients are hypertension, hypothyroidism, hyperlipidemia, hypogonadism
Alstrom Syndrome is an autosomal recessive, single gene disorder caused by mutations in ALMS1 (Chr 2p13), a novel gene of currently u …
The interplay between prolactin and cardiovascular disease.
Glezer A, Santana MR, Bronstein MD, Donato J Jr, Jallad RS. Glezer A, et al. Front Endocrinol (Lausanne). 2023 Jan 10;13:1018090. doi: 10.3389/fendo.2022.1018090. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36704037 Free PMC article. Review.
Regarding possible mechanisms for the association between hyperprolactinemia and CVD risk, they include a possible direct effect of PRL, hypogonadism, and even effects of DA treatment, independently of changes in PRL levels. ...More studies evaluating CVD risk in hyperprol …
Regarding possible mechanisms for the association between hyperprolactinemia and CVD risk, they include a possible direct effect of PRL, …
The Alstrom syndrome: is it a rare or unknown disease?
Maffei P, Munno V, Marshall JD, Scandellari C, Sicolo N. Maffei P, et al. Ann Ital Med Int. 2002 Oct-Dec;17(4):221-8. Ann Ital Med Int. 2002. PMID: 12532560 Review.
The Alstrom syndrome involves multiple organ systems with a complex interaction between pathways. ...The most frequent causes of death include hepatic dysfunction and congestive heart failure secondary to dilated cardiomyopathy. We have summarized our personal clini …
The Alstrom syndrome involves multiple organ systems with a complex interaction between pathways. ...The most frequent causes of deat …
Testosterone treatment longer than 1 year shows more effects on functional hypogonadism and related metabolic, vascular, diabetic and obesity parameters (results of the 2-year clinical trial).
Groti Antonič K, Antonič B, Žuran I, Pfeifer M. Groti Antonič K, et al. Aging Male. 2020 Dec;23(5):1442-1454. doi: 10.1080/13685538.2020.1793132. Epub 2020 Aug 26. Aging Male. 2020. PMID: 32844712 Clinical Trial.
OBJECTIVE: We evaluated long-term effects of testosterone undecanoate on glycemic control, metabolic syndrome, vascular function and morphology in obese men with functional hypogonadism (FH) and type 2 diabetes (T2D) in a 2-year prospective clinical trial. ...CONCLU …
OBJECTIVE: We evaluated long-term effects of testosterone undecanoate on glycemic control, metabolic syndrome, vascular function and …
Dilated cardiomyopathy and ovarian dysgenesis in a patient with Malouf syndrome: a case report.
Gersak K, Strgulc M, Gorjup V, Dolenc-Strazar Z, Jurcic V, Penny DJ, Fan Y. Gersak K, et al. Mol Med Rep. 2013 Nov;8(5):1311-4. doi: 10.3892/mmr.2013.1669. Epub 2013 Sep 5. Mol Med Rep. 2013. PMID: 24008991
In the present study, we report on the sporadic case of a young female with dilated cardiomyopathy, hypergonadotropic hypogonadism, a small chin, bilateral blepharoptosis, marfanoid elongated fingers and hypothyroidism. Malouf syndrome may be caused by hetero …
In the present study, we report on the sporadic case of a young female with dilated cardiomyopathy, hypergonadotropic hypogonadism
Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of Malouf syndrome.
Narahara K, Kamada M, Takahashi Y, Tsuji K, Yokoyama Y, Ninomiya S, Seino Y. Narahara K, et al. Am J Med Genet. 1992 Oct 1;44(3):369-73. doi: 10.1002/ajmg.1320440320. Am J Med Genet. 1992. PMID: 1488988 Review.
We describe an 18-year-old girl with ovarian dysgenesis, dilated cardiomyopathy, mild mental retardation, broad nasal base, blepharoptosis, and minor skeletal abnormalities. ...Our patient, although a sporadic case, supports the existence of Malouf syndrome....
We describe an 18-year-old girl with ovarian dysgenesis, dilated cardiomyopathy, mild mental retardation, broad nasal base, blepharop …
Reduced artery diameters in Klinefelter syndrome.
Foresta C, Caretta N, Palego P, Ferlin A, Zuccarello D, Lenzi A, Selice R. Foresta C, et al. Int J Androl. 2012 Oct;35(5):720-5. doi: 10.1111/j.1365-2605.2012.01269.x. Epub 2012 Apr 10. Int J Androl. 2012. PMID: 22489599
Various epidemiological studies in relatively large cohorts of patients with Klinefelter syndrome (KS) described the increased morbidity and mortality in these subjects. ...Klinefelter syndrome patients showed significantly reduced artery diameters in all districts …
Various epidemiological studies in relatively large cohorts of patients with Klinefelter syndrome (KS) described the increased morbid …
Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation.
McPherson E, Turner L, Zador I, Reynolds K, Macgregor D, Giampietro PF. McPherson E, et al. Am J Med Genet A. 2009 Feb 15;149A(4):567-72. doi: 10.1002/ajmg.a.32627. Am J Med Genet A. 2009. PMID: 19283854
A previously reported patient with an adjacent mutation (Ala57Pro) had "atypical Werner syndrome" with dilated cardiomyopathy, hypogonadism, and sloping shoulders. ...LMNA sequencing should be considered for patients presenting with dilated cardiomyopa …
A previously reported patient with an adjacent mutation (Ala57Pro) had "atypical Werner syndrome" with dilated cardiomyopathy, …
Cardiovascular abnormalities in Klinefelter syndrome.
Pasquali D, Arcopinto M, Renzullo A, Rotondi M, Accardo G, Salzano A, Esposito D, Saldamarco L, Isidori AM, Marra AM, Ruvolo A, Napoli R, Bossone E, Lenzi A, Baliga RR, Saccà L, Cittadini A. Pasquali D, et al. Int J Cardiol. 2013 Sep 30;168(2):754-9. doi: 10.1016/j.ijcard.2012.09.215. Epub 2012 Oct 23. Int J Cardiol. 2013. PMID: 23092857
BACKGROUND: Several epidemiological studies have demonstrated an increased mortality from cardiovascular causes in patients with Klinefelter Syndrome (KS). Little information is available about the nature of the underlying cardiovascular abnormalities. ...Forty-eight Kline …
BACKGROUND: Several epidemiological studies have demonstrated an increased mortality from cardiovascular causes in patients with Klinefelter …
24 results