Search Results

The longitudinal growth trajectory of children with congenital hypothyroidism during the first 3 years of life.

• Authors : Alinia T; Metabolic Liver Disease Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.; Hovsepian S

Subjects: Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/diagnosis ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/epidemiology; Humans

• Source: European journal of pediatrics [Eur J Pediatr] 2024 Sep; Vol. 183 (9), pp. 4123-4131. Date of Electronic Publication: 2024 Jul 10.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7603873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients.

• Authors : Özer Y; Department of Pediatric Endocrinology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey. .; Anık A

Subjects: Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/drug therapy ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/diagnosis ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/blood

• Source: Journal of endocrinological investigation [J Endocrinol Invest] 2024 Sep; Vol. 47 (9), pp. 2213-2224. Date of Electronic Publication: 2024 Mar 28.Publisher: Springer Country of Publication: Italy NLM ID: 7806594 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1720-8386

Record details

A case report on congenital hypothyroidism and alpha thalassemia in children with anemia and muscle damage as the main manifestation.

• Authors : Zhang Y; Department of Child Rehabilitation, Dali Bai Autonomous Prefecture People's Hospital, Dali, Yunnan, China.; Li X

Subjects: alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/complications ; alpha-Thalassemia*/alpha-Thalassemia*/alpha-Thalassemia*/diagnosis ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/complications

• Source: Medicine [Medicine (Baltimore)] 2024 Aug 16; Vol. 103 (33), pp. e39446.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN:

Record details

Genotype-Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TG Defects.

• Authors : Tanase-Nakao K; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.; Iwahashi-Odano M

Subjects: Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/genetics ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/diagnosis ; Thyroglobulin*/Thyroglobulin*/Thyroglobulin*/genetics

• Source: The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2024 Aug 13; Vol. 109 (9), pp. 2358-2365.Publisher: Oxford University Press Country of Publication: United States NLM ID: 0375362 Publication Model: Print Cited Medium: Internet ISSN:

Record details

Genetic etiology in patients diagnosed with congenital hypothyroidism with new-generation sequencing: A single-center experience.

• Authors : Aytaç Kaplan EH; Mersin City Training and Research Hospital, Pediatric Endocrinology, Mersin, Turkey. Electronic address: .; Mermer S

Subjects: Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/genetics ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/diagnosis ; High-Throughput Nucleotide Sequencing*

• Source: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [Arch Pediatr] 2024 Aug; Vol. 31 (6), pp. 374-379. Date of Electronic Publication: 2024 Jul 14.Publisher: Elsevier Country of Publication: France NLM ID: 9421356 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1769-664X

Record details

Congenital hypothyroidism

• Source: Funk & Wagnalls New World Encyclopedia. 2023, 1p.

Record details

Incidence and associated risk factors of congenital hypothyroidism among newborns in Hainan, China: a retrospective study.

• Authors : Zhao Z; Newborn Disease Screening Center, Hainan Women and Children's Medical Center, Haikou, China.; Shi H

Subjects: Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/epidemiology ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/diagnosis ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/etiology

• Source: Journal of pediatric endocrinology & metabolism : JPEM [J Pediatr Endocrinol Metab] 2024 Jun 25; Vol. 37 (8), pp. 709-714. Date of Electronic Publication: 2024 Jun 25 (Print Publisher: Walter de Gruyter Country of Publication: Germany NLM ID: 9508900 Publication Model: Electronic-Print Cited Medium: Internet ISSN:

Record details

A Novel Variant (p.Leu1054Arg) in ABCB11 Presenting with Progressive Familial Intrahepatic Cholestasis (PFIC) with Congenital Hypothyroidism.

• Authors : Agarwal S; Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur, Rajasthan, 342005, India.; Rajvanshi N

Subjects: Cholestasis, Intrahepatic*/Cholestasis, Intrahepatic*/Cholestasis, Intrahepatic*/genetics ; Cholestasis, Intrahepatic*/Cholestasis, Intrahepatic*/Cholestasis, Intrahepatic*/diagnosis ; ATP Binding Cassette Transporter, Subfamily B, Member 11*/ATP Binding Cassette Transporter, Subfamily B, Member 11*/ATP Binding Cassette Transporter, Subfamily B, Member 11*/genetics Cholestasis, progressive familial intrahepatic 1

• Source: Indian journal of pediatrics [Indian J Pediatr] 2024 Nov; Vol. 91 (11), pp. 1194. Date of Electronic Publication: 2024 Sep 14.Publisher: Dr. K. C. Chaudhuri Foundation, co-published by Springer India Country of Publication: India NLM ID: 0417442 Publication Model: Print-Electronic

Record details

Frequency of Mutations in the TPO Gene in Patients with Congenital Hypothyroidism Due to Dyshormonogenesis in Chile.

• Authors : Arteaga-Jacobo MC; Programa de Genética Humana, Institute of Biomedical Science (ICBM), Facultad de Medicina, Universidad de Chile, Santiago 8380453, Chile.; Roco-Videla Á

Subjects: Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/genetics ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/blood ; Iodide Peroxidase*/Iodide Peroxidase*/Iodide Peroxidase*/genetics

• Source: Medicina (Kaunas, Lithuania) [Medicina (Kaunas)] 2024 Jul 16; Vol. 60 (7). Date of Electronic Publication: 2024 Jul 16.Publisher: MDPI Country of Publication: Switzerland NLM ID: 9425208 Publication Model: Electronic Cited Medium: Internet ISSN: 1648-9144

Record details

TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism.

• Authors : Zhang HY; The Core Laboratory in Medical Center of Clinical Research, Department of Molecular Diagnostics & Endocrinology, Shanghai Ninth People's Hospital, State Key Laboratory of Medical Genomics, Shanghai Jiao Tong University School of Medicine, Shanghai, China.; Wu FY

Subjects: Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/diagnosis ; Congenital Hypothyroidism*/Congenital Hypothyroidism*/Congenital Hypothyroidism*/genetics; Humans

• Source: Annals of laboratory medicine [Ann Lab Med] 2024 Jul 01; Vol. 44 (4), pp. 343-353. Date of Electronic Publication: 2024 Mar 04.Publisher: Korean Society for Laboratory Medicine Country of Publication: Korea (South) NLM ID: 101571172 Publication Model: Print-Electronic Cited Medium:

Record details