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Year Number of Results
1949 1
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1971 4
1972 5
1973 3
1974 3
1975 18
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1980 41
1981 35
1982 30
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1984 68
1985 58
1986 72
1987 79
1988 99
1989 109
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1992 168
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1999 289
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2001 300
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2003 395
2004 425
2005 514
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2007 551
2008 644
2009 686
2010 754
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2013 964
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20,203 results

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Quoted phrase not found in phrase index: "Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome"
Page 1
The trisomy 18 syndrome.
Cereda A, Carey JC. Cereda A, et al. Orphanet J Rare Dis. 2012 Oct 23;7:81. doi: 10.1186/1750-1172-7-81. Orphanet J Rare Dis. 2012. PMID: 23088440 Free PMC article. Review.
The trisomy 18 syndrome, also known as Edwards syndrome, is a common chromosomal disorder due to the presence of an extra chromosome 18, either full, mosaic trisomy, or partial trisomy 18q. ...Typical minor anomalies include characteristic craniofacial features, cle …
The trisomy 18 syndrome, also known as Edwards syndrome, is a common chromosomal disorder due to the presence of an extra chro …
Post-finasteride syndrome.
Pereira AFJR, Coelho TOA. Pereira AFJR, et al. An Bras Dermatol. 2020 May-Jun;95(3):271-277. doi: 10.1016/j.abd.2020.02.001. Epub 2020 Mar 25. An Bras Dermatol. 2020. PMID: 32317131 Free PMC article.
Recently there have been reports of adverse drug-related reactions that persisted for at least three months after discontinuation of this drug, and the term post-finasteride syndrome arose. It includes persistent sexual, neuropsychiatric, and physical symptoms. Studies to …
Recently there have been reports of adverse drug-related reactions that persisted for at least three months after discontinuation of this dr …
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature.
Fan X, Zhao S, Yu C, Wu D, Yan Z, Fan L, Song Y, Wang Y, Li C, Ming Y, Gui B, Niu Y, Li X, Yang X, Luo S, Zhang Q, Zhao X, Pan H, Li M, Xia W, Qiu G, Liu P, Zhang S, Zhang J, Wu Z; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Lupski JR, Posey JE, Chen S, Gong C, Wu N. Fan X, et al. J Genet Genomics. 2021 May 20;48(5):396-402. doi: 10.1016/j.jgg.2021.02.008. Epub 2021 Mar 22. J Genet Genomics. 2021. PMID: 34006472
All patients were retrospectively divided into two groups: an isolated short stature group (group I, n = 257) and an apparently syndromic short stature group (group II, n = 304). ...Genes involved in fundamental cellular process played an important role in th …
All patients were retrospectively divided into two groups: an isolated short stature group (group I, n = 257) and an apparently sy …
The Role of Telomeres in Human Disease.
Armanios M. Armanios M. Annu Rev Genomics Hum Genet. 2022 Aug 31;23:363-381. doi: 10.1146/annurev-genom-010422-091101. Epub 2022 Jun 24. Annu Rev Genomics Hum Genet. 2022. PMID: 35609925 Free PMC article. Review.
Telomere biology was first studied in maize, ciliates, yeast, and mice, and in recent decades, it has informed understanding of common disease mechanisms with broad implications for patient care. Short telomere syndromes are the most prevalent premature aging disord …
Telomere biology was first studied in maize, ciliates, yeast, and mice, and in recent decades, it has informed understanding of common disea …
Sleep disturbance and cancer-related fatigue symptom cluster in breast cancer patients undergoing chemotherapy.
Fox RS, Ancoli-Israel S, Roesch SC, Merz EL, Mills SD, Wells KJ, Sadler GR, Malcarne VL. Fox RS, et al. Support Care Cancer. 2020 Feb;28(2):845-855. doi: 10.1007/s00520-019-04834-w. Epub 2019 Jun 3. Support Care Cancer. 2020. PMID: 31161437 Free PMC article.
Latent profile analysis was used to derive groups of patients at each timepoint who scored similarly on percent of the day/night asleep per actigraphy, the Pittsburgh Sleep Quality Index global score, and the five subscales of the Multidimensional Fatigue Symptom Inventory-Sho …
Latent profile analysis was used to derive groups of patients at each timepoint who scored similarly on percent of the day/night asleep per …
Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report.
Brugada P, Brugada J. Brugada P, et al. J Am Coll Cardiol. 1992 Nov 15;20(6):1391-6. doi: 10.1016/0735-1097(92)90253-j. J Am Coll Cardiol. 1992. PMID: 1309182 Free article.
The arrhythmia leading to (aborted) sudden death was a rapid polymorphic ventricular tachycardia initiating after a short coupled ventricular extrasystole. A similar arrhythmia was initiated by two to three ventricular extrastimuli in four of the seven patients studied by …
The arrhythmia leading to (aborted) sudden death was a rapid polymorphic ventricular tachycardia initiating after a short coupled ven …
Early rehabilitation to prevent postintensive care syndrome in patients with critical illness: a systematic review and meta-analysis.
Fuke R, Hifumi T, Kondo Y, Hatakeyama J, Takei T, Yamakawa K, Inoue S, Nishida O. Fuke R, et al. BMJ Open. 2018 May 5;8(5):e019998. doi: 10.1136/bmjopen-2017-019998. BMJ Open. 2018. PMID: 29730622 Free PMC article.
INTRODUCTION: We examined the effectiveness of early rehabilitation for the prevention of postintensive care syndrome (PICS), characterised by an impaired physical, cognitive or mental health status, among survivors of critical illness. ...Early rehabilitation did not impr …
INTRODUCTION: We examined the effectiveness of early rehabilitation for the prevention of postintensive care syndrome (PICS), charact …
Stroke warning syndromes.
Sen A, Birns J, Bhalla A. Sen A, et al. Br J Hosp Med (Lond). 2020 Jan 2;81(1):1-5. doi: 10.12968/hmed.2019.0222. Epub 2020 Jan 28. Br J Hosp Med (Lond). 2020. PMID: 32003622
Stroke warning syndromes present as stereotypical, recurrent transient episodes of focal neurological deficit, in the absence of cortical signs, occurring within a short period of time. They are broadly divided into two main subtypes, based on vascular territory: ca …
Stroke warning syndromes present as stereotypical, recurrent transient episodes of focal neurological deficit, in the absence of cort …
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. ...The life span of patients with Alstrom Syndrome rarely exceeds 40 years. There is no specific therapy f …
Alstrom Syndrome is an autosomal recessive, single gene disorder caused by mutations in ALMS1 (Chr 2p13), a novel gene of currently u …
The Role of Pelvic Floor Muscle Training on Low Anterior Resection Syndrome: A Multicenter Randomized Controlled Trial.
Asnong A, D'Hoore A, Van Kampen M, Wolthuis A, Van Molhem Y, Van Geluwe B, Devoogdt N, De Groef A, Guler Caamano Fajardo I, Geraerts I. Asnong A, et al. Ann Surg. 2022 Nov 1;276(5):761-768. doi: 10.1097/SLA.0000000000005632. Epub 2022 Jul 27. Ann Surg. 2022. PMID: 35894434 Free PMC article. Clinical Trial.
BACKGROUND AND OBJECTIVE: Total mesorectal excision (TME) for rectal cancer (RC) often results in significant bowel symptoms, commonly known as low anterior resection syndrome (LARS). Although pelvic floor muscle training (PFMT) is recommended in noncancer populations for …
BACKGROUND AND OBJECTIVE: Total mesorectal excision (TME) for rectal cancer (RC) often results in significant bowel symptoms, commonly known …
20,203 results
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