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

Year Number of Results
1964 1
1973 1
1974 1
1975 6
1979 1
1980 2
1981 2
1983 1
1984 1
1985 3
1986 2
1987 1
1988 1
1989 1
1990 1
1991 4
1992 2
1993 2
1994 4
1995 1
1996 1
1997 3
1999 2
2000 2
2001 9
2002 3
2003 3
2004 3
2005 6
2006 9
2007 4
2008 9
2009 5
2010 3
2011 5
2012 7
2013 7
2014 3
2015 7
2016 4
2017 5
2018 5
2019 10
2020 9
2021 9
2022 8
2023 5
2024 5

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170 results

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The following terms were not found in PubMed: 20Won, 20Hong
Page 1
Prader-Willi syndrome.
Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Cassidy SB, et al. Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26. Genet Med. 2012. PMID: 22237428 Free article. Review.
Prader-Willi syndrome is characterized by severe infantile hypotonia with poor suck and failure to thrive; hypogonadism causing genital hypoplasia and pubertal insufficiency; characteristic facial features; early-childhood onset obesity and hyperphagia; developmental delay …
Prader-Willi syndrome is characterized by severe infantile hypotonia with poor suck and failure to thrive; hypogonadism causing genit …
Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
Angulo MA, Butler MG, Cataletto ME. Angulo MA, et al. J Endocrinol Invest. 2015 Dec;38(12):1249-63. doi: 10.1007/s40618-015-0312-9. Epub 2015 Jun 11. J Endocrinol Invest. 2015. PMID: 26062517 Free PMC article. Review.
There are three main genetic subtypes in PWS: paternal 15q11-q13 deletion (65-75 % of cases), maternal uniparental disomy 15 (20-30 % of cases), and imprinting defect (1-3 %). DNA methylation analysis is the only technique that will diagnose PWS in all three molecular gene …
There are three main genetic subtypes in PWS: paternal 15q11-q13 deletion (65-75 % of cases), maternal uniparental disomy 15 (20-30 % …
KCNK9 Imprinting Syndrome.
Zadeh N, Graham JM Jr. Zadeh N, et al. 2017 Mar 23. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2017 Mar 23. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 28333430 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: KCNK9 imprinting syndrome is characterized by congenital central hypotonia (manifest as decreased movement, lethargy, and weak cry), severe feeding difficulties (resulting from facial weakness and poor suck), delayed development/intellectual disab …
CLINICAL CHARACTERISTICS: KCNK9 imprinting syndrome is characterized by congenital central hypotonia (manifest as decreased movement, lethar …
Oral galactagogues (natural therapies or drugs) for increasing breast milk production in mothers of non-hospitalised term infants.
Foong SC, Tan ML, Foong WC, Marasco LA, Ho JJ, Ong JH. Foong SC, et al. Cochrane Database Syst Rev. 2020 May 18;5(5):CD011505. doi: 10.1002/14651858.CD011505.pub2. Cochrane Database Syst Rev. 2020. PMID: 32421208 Free PMC article.
When addressing this concern, it is important first to consider the influence of maternal and neonatal health, infant suck, proper latch, and feeding frequency on milk production, and that steps be taken to correct or compensate for any contributing issues. ...Only one stu …
When addressing this concern, it is important first to consider the influence of maternal and neonatal health, infant suck, proper la …
Vitamin B12 Deficiency in Infants.
Akcaboy M, Malbora B, Zorlu P, Altınel E, Oguz MM, Senel S. Akcaboy M, et al. Indian J Pediatr. 2015 Jul;82(7):619-24. doi: 10.1007/s12098-015-1725-3. Epub 2015 Apr 5. Indian J Pediatr. 2015. PMID: 25840526
The most common symptoms of the patients were; infections in 30 %, pallor in 25 %, hypotonia and neuro-developmental delay in 25 %, refusal to solid food or to suck in 20 %, failure to thrive in 15 %, fatigue in 10 %. Twenty-five percent of patients had neurologic s …
The most common symptoms of the patients were; infections in 30 %, pallor in 25 %, hypotonia and neuro-developmental delay in 25 %, refusal …
Development of an IgY-Based Treatment to Control Bovine Coronavirus Diarrhea in Dairy Calves.
Bok M, Vega CG, Castells M, Colina R, Wigdorovitz A, Parreño V. Bok M, et al. Viruses. 2023 Mar 9;15(3):708. doi: 10.3390/v15030708. Viruses. 2023. PMID: 36992417 Free PMC article.
Standard practice dictates that to prevent BCoV diarrhea, dams should be immunized in the last stage of pregnancy to increase BCoV-specific antibody (Ab) titers in serum and colostrum. For the prevention to be effective, calves need to suck maternal colostrum within the fi …
Standard practice dictates that to prevent BCoV diarrhea, dams should be immunized in the last stage of pregnancy to increase BCoV-specific …
An abnormal finding in the third trimester.
Marshall H, Petrie K. Marshall H, et al. Arch Dis Child Educ Pract Ed. 2021 Oct;106(5):289-291. doi: 10.1136/archdischild-2019-317455. Epub 2019 Dec 10. Arch Dis Child Educ Pract Ed. 2021. PMID: 31822484
A healthy woman presented with an antepartum haemorrhage at 35/40 during a low-risk pregnancy with normal antenatal bloods and anomaly scan at 20/40 gestation. Following an abnormal ultrasound (USS), the baby was delivered by emergency C-section. A male infant was born in …
A healthy woman presented with an antepartum haemorrhage at 35/40 during a low-risk pregnancy with normal antenatal bloods and anomaly scan …
Variability in Swallowing Biomechanics in Infants with Feeding Difficulties: A Videofluoroscopic Analysis.
Fuller L, Miles A, Dharmarathna I, Allen J. Fuller L, et al. Dysphagia. 2022 Dec;37(6):1740-1747. doi: 10.1007/s00455-022-10436-2. Epub 2022 Mar 17. Dysphagia. 2022. PMID: 35298686 Free PMC article.
Our research questions were as follows: Is it possible to assess swallow to swallow variability in an infant with feeding concerns, is there variability in pharyngeal timing and displacement in infants referred for videofluoroscopy, and is variability associated with aspiration r …
Our research questions were as follows: Is it possible to assess swallow to swallow variability in an infant with feeding concerns, is there …
Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.
Butler MG, Manzardo AM, Forster JL. Butler MG, et al. Curr Pediatr Rev. 2016;12(2):136-66. doi: 10.2174/1573396312666151123115250. Curr Pediatr Rev. 2016. PMID: 26592417 Free PMC article. Review.
These include paternal 15q11-q13 deletion (about 70% of cases), maternal uniparental disomy 15 or both 15s from the mother (20-30% of cases), and defects in the imprinting center (1-3%) which controls the expression of imprinted genes in this chromosome region. Clinical ma …
These include paternal 15q11-q13 deletion (about 70% of cases), maternal uniparental disomy 15 or both 15s from the mother (20-30% of …
Endoscopic Ultrasonic Aspiration of Brain Abscess.
Spennato P, Imperato A, Scala MR, Di Costanzo M, Ruggiero C, Cinalli G. Spennato P, et al. World Neurosurg. 2024 Apr;184:1-2. doi: 10.1016/j.wneu.2023.12.127. Epub 2023 Dec 29. World Neurosurg. 2024. PMID: 38160908
We present the case of an 11-year-old boy affected by a parieto-occipital brain abscess and initial ventriculitis who underwent endoscopic surgery. An ultrasonic aspirator was used to wash and suck the purulent material and fragment and remove the more solid fibrinoid comp …
We present the case of an 11-year-old boy affected by a parieto-occipital brain abscess and initial ventriculitis who underwent endoscopic s …
170 results