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

Year Number of Results
1986 1
1994 1
1995 2
1997 1
1999 3
2001 1
2002 2
2003 3
2004 1
2005 3
2006 4
2007 2
2008 5
2009 3
2011 4
2012 4
2013 3
2014 4
2016 3
2017 5
2018 6
2019 2
2020 3
2021 3
2022 4
2023 4
2024 0

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69 results

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Page 1
Pediatric Hypothyroidism: Diagnosis and Treatment.
Wassner AJ. Wassner AJ. Paediatr Drugs. 2017 Aug;19(4):291-301. doi: 10.1007/s40272-017-0238-0. Paediatr Drugs. 2017. PMID: 28534114 Review.
Similarly, the diagnosis and treatment of severe acquired hypothyroidism is straightforward and clearly of clinical benefit, but uncertainty remains about the optimal management of mild subclinical hypothyroidism. This review summarizes current knowledge of the causes, cli …
Similarly, the diagnosis and treatment of severe acquired hypothyroidism is straightforward and clearly of clinical benefit, but uncertainty …
Attention Deficit Hyperactivity and Autism Spectrum Disorders as the Core Symptoms of AUTS2 Syndrome: Description of Five New Patients and Update of the Frequency of Manifestations and Genotype-Phenotype Correlation.
Sanchez-Jimeno C, Blanco-Kelly F, López-Grondona F, Losada-Del Pozo R, Moreno B, Rodrigo-Moreno M, Martinez-Cayuelas E, Riveiro-Alvarez R, Fenollar-Cortés M, Ayuso C, Rodríguez de Alba M, Lorda-Sanchez I, Almoguera B. Sanchez-Jimeno C, et al. Genes (Basel). 2021 Aug 30;12(9):1360. doi: 10.3390/genes12091360. Genes (Basel). 2021. PMID: 34573342 Free PMC article. Review.
The phenotype of the patients was characterized by attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) or autistic features and mild global developmental delay (GDD) or intellectual disability (ID), all in 4/5 patients (80%), a frequency high …
The phenotype of the patients was characterized by attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) or aut …
Neonatal screening for primary and central congenital hypothyroidism: is it time to go Dutch?
Boelen A, Zwaveling-Soonawala N, Heijboer AC, van Trotsenburg ASP. Boelen A, et al. Eur Thyroid J. 2023 Jul 27;12(4):e230041. doi: 10.1530/ETJ-23-0041. Eur Thyroid J. 2023. PMID: 37326450 Free PMC article. Review.
Although the necessity of central CH detection by NBS is still under debate, it has been shown that most central CH patients have moderate-to-severe hypothyroidism instead of mild and that early detection of central CH by NBS probably improves its clinical outcome and clin …
Although the necessity of central CH detection by NBS is still under debate, it has been shown that most central CH patients have moderate-t …
Diagnosis and management of disorders of IGF-I synthesis and action.
Wit JM. Wit JM. Pediatr Endocrinol Rev. 2011 Sep;9 Suppl 1:538-40. Pediatr Endocrinol Rev. 2011. PMID: 22423513 Review.
After a proper medical history, growth analysis and physical examination of a short child, followed by radiological and laboratory screening, the clinician may decide to perform genetic testing. ...IGF-I resistance is seen in heterozygous defects of IGF1R. If besides sh …
After a proper medical history, growth analysis and physical examination of a short child, followed by radiological and laboratory sc …
Diagnosis, treatment and outcome of congenital hypothyroidism.
Van Vliet G, Deladoëy J. Van Vliet G, et al. Endocr Dev. 2014;26:50-9. doi: 10.1159/000363155. Epub 2014 Aug 29. Endocr Dev. 2014. PMID: 25231444 Review.
Transition to adult care is particularly important for females, who should receive counseling about increased levothyroxine needs during future pregnancies. Cognitive outcome has improved dramatically with screening for overt congenital hypothyroidism, but the benefits fro …
Transition to adult care is particularly important for females, who should receive counseling about increased levothyroxine needs dur …
Neonatal screening for congenital hypothyroidism.
Torresani T. Torresani T. Endocr Dev. 2014;26:44-9. doi: 10.1159/000363154. Epub 2014 Aug 29. Endocr Dev. 2014. PMID: 25231443 Review.
The possibility of measuring thyroid hormones from blood dried on filter paper opened the way to identifying neonates with congenital hypothyroidism (CH) already in the first days of life. Consequently the early initiation of adequate replacement therapy opened the way to …
The possibility of measuring thyroid hormones from blood dried on filter paper opened the way to identifying neonates with congenital hypoth …
Detection and treatment of congenital hypothyroidism.
Grüters A, Krude H. Grüters A, et al. Nat Rev Endocrinol. 2011 Oct 18;8(2):104-13. doi: 10.1038/nrendo.2011.160. Nat Rev Endocrinol. 2011. PMID: 22009163 Review.
Controversy exists regarding the necessity to adjust current screening programs to also diagnose patients with central hypothyroidism or those with mild forms of congenital hypothyroidism, who have high TSH levels but normal T(4) and normal T(3) levels (also known as 'subc …
Controversy exists regarding the necessity to adjust current screening programs to also diagnose patients with central hypothyroidism or tho …
Newborn Screening in the US May Miss Mild Persistent Hypothyroidism.
Kilberg MJ, Rasooly IR, LaFranchi SH, Bauer AJ, Hawkes CP. Kilberg MJ, et al. J Pediatr. 2018 Jan;192:204-208. doi: 10.1016/j.jpeds.2017.09.003. J Pediatr. 2018. PMID: 29246344 Free PMC article.
This approach will miss congenital hypothyroidism in infants with persistent mild TSH elevations. We recommend that all NBS programs provide age-adjusted TSH cutoffs, and suggest developing a standard approach to screening for congenital hypothyroidism in the US....
This approach will miss congenital hypothyroidism in infants with persistent mild TSH elevations. We recommend that all NBS programs …
Novel insight into etiology, diagnosis and management of primary adrenal insufficiency.
Malikova J, Flück CE. Malikova J, et al. Horm Res Paediatr. 2014;82(3):145-57. doi: 10.1159/000363107. Epub 2014 Aug 1. Horm Res Paediatr. 2014. PMID: 25096886 Free article. Review.
Newer work has also expanded the genetic causes underlying isolated, familial glucocorticoid deficiency (FGD). Mild mutations of CYP11A1 or StAR have been identified in patients with FGD. MCM4 mutations were found in a variant of FGD in an Irish travelling community manife …
Newer work has also expanded the genetic causes underlying isolated, familial glucocorticoid deficiency (FGD). Mild mutations of CYP1 …
Clinical survey of current practice regarding treatment of children with borderline thyroid abnormalities.
Lain S, Nassar N, Jack M. Lain S, et al. J Paediatr Child Health. 2023 Jan;59(1):129-133. doi: 10.1111/jpc.16259. Epub 2022 Oct 27. J Paediatr Child Health. 2023. PMID: 36303462 Free PMC article.
AIM: Recently, there has been debate about reducing newborn screening (NBS) thyroid-stimulating hormone (TSH) cut-offs to identify children with mild, but potentially clinically significant, thyroid deficiency. ...CONCLUSION: This contemporary survey of clinicians regardin …
AIM: Recently, there has been debate about reducing newborn screening (NBS) thyroid-stimulating hormone (TSH) cut-offs to identify children …
69 results