Update Research and References of Congenital Hypothyroidism 2013

Update Research and References of Congenital Hypothyroidism 2013

  • Prevalence of disorders detected by newborn screening in Santa Catarina]. Nunes AK, Wachholz RG, Rover MR, Souza LC. Arq Bras Endocrinol Metabol. 2013 Jul;57(5):360-7.
  • Neurodevelopmental and body composition outcomes in children with congenital hypothyroidism treated with high-dose initial replacement and close monitoring. Albert BB, Heather N, Derraik JG, Cutfield WS, Wouldes T, Tregurtha S, Mathai S, Webster D, Jefferies C, Gunn AJ, Hofman PL. J Clin Endocrinol Metab. 2013 Jul 16.
  • Permanent and transient congenital hypothyroidism in fayoum, egypt: a descriptive retrospective study. Bekhit OE, Yousef RM. PLoS One. 2013 Jun 28;8(6):e68048.
  • Fasting glucagon-like peptide-1 in patients with overt hyperthyroidism and euthyroid congenital hypothyroidism. Cheng JP, Yue HN, Ma SG, Jin Y, Xu W, Bai F. J Pediatr Endocrinol Metab. 2013 Jul 6:1-5.
  • Risk factors for congenital hypothyroidism in Egypt: results of a population case-control study (2003-2010). Abdelmoktader AM. Ann Saudi Med. 2013 May-Jun;33(3):273-6.
  • Newborn Screening for Congenital Hypothyroidism. Clause M. J Pediatr Nurs. 2013 Jun 19.
  • A Retrospective Review of Newborn Screening for Congenital Hypothyroidism and Newborn Thyroid Disease at a Major Medical Center. Cameo T, Gumer LB, Williams KM, Gomez J, McMahon DJ, Oberfield SE. Clin Pediatr (Phila). 2013 Jun 18. [Epub ahead of print]
  • Factors associated with hearing impairment in patients with congenital hypothyroidism treated since the neonatal period: a national population-based study. Lichtenberger-Geslin L, Dos Santos S, Hassani Y, Ecosse E, Van Den Abbeele T, Léger J. J Clin Endocrinol Metab. 2013 Jun 18.
  • Hirsutism: A Clinico-investigative Study. Chhabra S, Gautam RK, Kulshreshtha B, Prasad A, Sharma N. Int J Trichology. 2012 Oct;4(4):246-50.
  • Maternal-fetal thyroid function at the time of birth and its relation with iodine intake. Velasco I, Martin J, Gallego M, Gutierrez-Repiso C, Santiago P, Lopez-Siguero JP, Gonzalez Mesa E, Herrera Peral J, Perez V, Garcia-Fuentes E, Soriguer-Escofet F. Thyroid. 2013 Jun 13.
  • Iodine deficiency, thyroid function and hearing deficit: a review. Melse-Boonstra A, Mackenzie I. Nutr Res Rev. 2013 Jun 12:1-8
  • TPO genetic variants and risk of differentiated thyroid carcinoma in two European populations. Cipollini M, Pastor S, Gemignani F, Castell J, Garritano S, Bonotti A, Biarnés J, Figlioli G, Romei C, Marcos R, Cristaudo A, Elisei R, Landi S, Velázquez A. Int J Cancer. 2013 Jun 10.
  • A levothyroxine dose recommendation for the treatment of children and adolescents with autoimmune thyroiditis induced hypothyroidism. Ellerbroek V, Warncke K, Köhle J, Bonfig W. J Pediatr Endocrinol Metab. 2013 Jun 8:1-6
  • Lissencephaly presenting with congenital hypothyroidism. Kumar S, Suthar R, Panigrahi I, Marwaha RK. J Pediatr Endocrinol Metab. 2013 Jun 8:1-3.
  • Maternal and neonatal urinary iodine status and its effect on neonatal TSH levels in a mildly iodine-deficient area. Yaman AK, Demirel F, Ermiş B, Pişkin IE. J Clin Res Pediatr Endocrinol. 2013;5(2):90-4.
  • Establishment and development of a national newborn screening programme for congenital hypothyroidism in Turkey. Dilli D, Çzbaş S, Acıcan D, Yamak N, Ertek M, Dilmen U. J Clin Res Pediatr Endocrinol. 2013;5(2):73-9
  • A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the Thyroid peroxidase Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter. Lee CC, Harun F, Jalaludin MY, Heh CH, Othman R, Mat Junit S. Int J Endocrinol. 2013;2013:987186.
  • Dominant protein interactions that influence the pathogenesis of conformational diseases. Wright J, Wang X, Haataja L, Kellogg AP, Lee J, Liu M, Arvan P. J Clin Invest. 2013 Jul 1;123(7):3124-34.
  • Septo-optic dysplasia: fitting the pieces together. Ferraria N, Castro S, Amaral D, Lopes L. BMJ Case Rep. 2013 May 24;2013.
  • The molecular causes of thyroid dysgenesis: a systematic review. Nettore IC, Cacace V, De Fusco C, Colao A, Macchia PE. J Endocrinol Invest. 2013 May 22.
  • Topete-González LR, Ramirez-Garcia SA, Macías-López GG, Troyo-Sanromán R, Ramos-Ramírez IM, Elizondo-Rueda ME, Dávalos-Rodríguez N, González-Gamez JG, Cabrera-Pivaral CE. Rev Med Inst Mex Seguro Soc. 2013 Mar-Apr;51(2):136-41
  • Congenital hypothyroidism alters the oxidative status, enzyme activities and morphological parameters in the hippocampus of developing rats. Cattani D, Goulart PB, Cavalli VL, Winkelmann-Duarte E, Dos Santos AQ, Pierozan P, de Souza DF, Woehl VM, Fernandes MC, Silva FR, Gonçalves CA, Pessoa-Pureur R, Zamoner A. Mol Cell Endocrinol. 2013 Aug 15;375(1-2):14-26.
  • Congenital hypothyroidism screening program in Turkey: a local evaluation. Kuşdal Y, Yeşiltepe-Mutlu G, Ozsu E, Cizmecioğlu FM, Hatun S. Turk J Pediatr. 2012 Nov-Dec;54(6):590-5.
  • Congenital hypothyroidism: recommendations of the Thyroid Department of the Brazilian Society of Endocrinology and Metabolism. Maciel LM, Kimura ET, Nogueira CR, Mazeto GM, Magalhães PK, Nascimento ML, Nesi-França S, Vieira SE. Arq Bras Endocrinol Metabol. 2013 Apr;57(3):184-92.
  • A boy with prepubertal gynecomastia, hyperprolactinemia, and hypothyroidism. Dayal D, Bhalla AK, Sachdeva N. J Pediatr Endocrinol Metab. 2013;26(3-4):357-60.
  • Chorea due to TITF1/NKX2-1 mutation: phenotypical description and therapeutic response in a family]. Salvado M, Boronat-Guerrero S, Hernández-Vara J, Álvarez-Sabin J. Rev Neurol. 2013 May 16;56(10):515-20.
  • Asn441 plays a key role in folding and function of the Na+/I- symporter (NIS). Li W, Nicola JP, Amzel LM, Carrasco N. FASEB J. 2013 Aug;27(8):3229-38.
  • Combined l-thyroxine and l-triiodothyronine replacement therapy in congenital hypothyroidism]. Péter F, Muzsnai A. Orv Hetil. 2013 May 12;154(19):738-44.
  • A NEW PAX8 MUTATION CAUSING CONGENITAL HYPOTHYROIDISM IN THREE GENERATIONS OF A FAMILY IS ASSOCIATED WITH ABNORMALITIES IN THE UROGENITAL TRACT. Carvalho A, Hermanns P, Rodrigues AL, Cabral R, Bikker H, Sousa I, Anselmo JD, Pereira-Duarte C, Mota-Vieira L, Pohlenz J. Thyroid. 2013 May 7.
  • Goiter: a rare cause of childhood dyspnea]. Duhamel A, Grevent D, Nouyrigat V, Cheron G. Arch Pediatr. 2013 Jun;20(6):661-4
  • Analysis of EphA5 receptor in the developing rat brain: an in vivo study in congenital hypothyroidism model. Wu YJ, Xu MY, Wang L, Sun BL, Gu GX. Eur J Pediatr. 2013 Aug;172(8):1077-83
  • Thyroid Function from Birth to Adolescence in Prader-Willi Syndrome. Sharkia M, Michaud S, Berthier MT, Giguère Y, Stewart L, Deladoëy J, Deal C, Van Vliet G, Chanoine JP. J Pediatr. 2013 Apr 25
  • Genome wide analysis in a discordant monozygotic twin with caudal appendage and multiple congenital anomalies. Cogulu O, Pariltay E, Koroglu OA, Aykut A, Ozyurek R, Levent E, Kultursay N, Ozkinay F. Genet Couns. 2013;24(1):85-91.
  • Early adiposity rebound and obesity in children with congenital hypothyroidism. Chen SY, Lin SJ, Lin SH, Chou YY. Pediatr Neonatol. 2013 Apr;54(2):107-12.
  • Measuring free thyroxine levels in neonatal heel-prick samples. Boelen A, van Veen M, Verkerk PH, Diependaal G, Loeber G, Elvers B, Endert E. Clin Chim Acta. 2013 Aug 23;423:51-5.
  • Congenital hypothyroidism secondary to thyroid hypoplasia detected in adulthood]. Monti P, Roveto S, Rajuan S, Gazzi C, Rimoldi D. Medicina (B Aires). 2013;73(2):145-7
  • Effect of nitrate and L-arginine therapy on nitric oxide levels in serum, heart, and aorta of fetal hypothyroid rats. Ghasemi A, Mehrazin F, Zahediasl S. J Physiol Biochem. 2013 Apr 9.
  • Cretinism revisited. Srivastav A, Maisnam I, Dutta D, Ghosh S, Mukhopadhyay S, Chowdhury S. Indian J Endocrinol Metab. 2012 Dec;16(Suppl 2):S336-7
  • Subclinical hypothyroidism in children. Seshadri KG. Indian J Endocrinol Metab. 2012 Dec;16(Suppl 2):S156-8. doi: 10.4103/2230-8210.104028.
  • Congenital hypothyroidism: Screening dilemma. Desai MP. Indian J Endocrinol Metab. 2012 Dec;16(Suppl 2):S153-5
  • Congenital proprotein convertase 1/3 deficiency causes malabsorptive diarrhea and other endocrinopathies in a pediatric cohort. Martín MG, Lindberg I, Solorzano-Vargas RS, Wang J, Avitzur Y, Bandsma R, Sokollik C, Lawrence S, Pickett LA, Chen Z, Egritas O, Dalgic B, Albornoz V, de Ridder L, Hulst J, Gok F, Aydoğan A, Al-Hussaini A, Gok DE, Yourshaw M, Wu SV, Cortina G, Stanford S, Georgia S. Gastroenterology. 2013 Jul;145(1):138-48.
  • Changes of red blood cell rheology in newborns with congenital hypothyroidism during treatment. Akin MA, Aydogan S, Gunes T, Artis AS, Karakukcu M, Kurtoglu S.  J Matern Fetal Neonatal Med. 2013 May 7.
  • Imaging criteria for categorizing congenital hypothyroidism into thyroid hypoplasia and dyshormonogenesis subtypes. Boughattas S, Abdullah M, Al Nammi A. Radiology. 2013 Apr;267(1):313-4
  • Side effects and risk profile of lithium : Critical assessment of a systematic review and meta-analysis]. Bschor T, Bauer M. Nervenarzt. 2013 Jul;84(7):860-3. 3766-z
  • Evolution of the neonatal screening program in the state of Tocantins]. Mendes LC, dos Santos TT, Bringel Fde A. Arq Bras Endocrinol Metabol. 2013 Mar;57(2):112-9.
  • Hypothyroidism compromises hypothalamic leptin signaling in mice. Groba C, Mayerl S, van Mullem AA, Visser TJ, Darras VM, Habenicht AJ, Heuer H. Mol Endocrinol. 2013 Apr;27(4):586-97.
  • Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutations. Altmann K, Hermanns P, Mühlenberg R, Fricke-Otto S, Wentzell R, Pohlenz J. Exp Clin Endocrinol Diabetes. 2013 Jun;121(6):343-6.
  • Growth and specialized growth charts of children with congenital hypothyroidism detected by neonatal screening in isfahan, iran. Feizi A, Hashemipour M, Hovsepian S, Amirkhani Z, Kelishadi R, Yazdi M, Heydari K, Sajadi A, Amini M. ISRN Endocrinol. 2013;2013:463939.
  • A review of the embryological development and associated developmental abnormalities of the sternum in the light of a rare palaeopathological case of sternal clefting. van der Merwe AE, Weston DA, Oostra RJ, Maat GJ. Homo. 2013 Apr;64(2):129-41
  • L-thyroxine therapy and growth processes in children with Down syndrome. Kowalczyk K, Pukajło K, Malczewska A, Król-Chwastek A, Barg E. Adv Clin Exp Med. 2013 Jan-Feb;22(1):85-92.
  • Effects of hypothyroidism on expression of CRMP2B and ARPC5 during development of the rat frontal cortex. Liu CR, Miao J, Zhang YL, Liu YM, Yu BG. Int J Biol Sci. 2013;9(2):209-18.
  • Treating congenital hypothyroidism–which levothyroxine? Deladoëy J, Van Vliet G. Nat Rev Endocrinol. 2013 May;9(5):257-8
  • Prenatal diagnosis and treatment perspective of fetal hypothyroidism with goiter. Gulraze A, Kurdi W, Tulbah M, Niaz FA. J Coll Physicians Surg Pak. 2013 Mar;23(3):216-8.
  • Congenital hypothyroidism presenting with postpartum bradycardia. Kara S, Tayman C, Tonbul A, Andiran N, Tatli M, Türkay S. J Coll Physicians Surg Pak. 2013 Mar;23(3):214-5.
  • Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene. Yoshizawa-Ogasawara A, Ogikubo S, Satoh M, Narumi S, Hasegawa T. J Pediatr Endocrinol Metab. 2013;26(1-2):45-52.
  • The prevalence of Iodine Deficiency Disorder in two different populations in northern province of Iran: a comparison using different indicators recommended by WHO. Dalili S, Mohtasham-Amiri Z, Rezvani SM, Dadashi A, Medghalchi A, Hoseini S, Gholami-Nezhad H, Amirhaki A. Acta Med Iran. 2012;50(12):822-6.
  • Congenital hypothyroidism caused by a novel homozygous mutation in the thyroglobulin gene. Agretti P, De Marco G, Di Cosmo C, Ferrarini E, Montanelli L, Bagattini B, Vitti P, Tonacchera M. Eur J Pediatr. 2013 Jul;172(7):959-64
  • Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism. Olivieri A, Corbetta C, Weber G, Vigone MC, Fazzini C, Medda E; Italian Study Group for Congenital Hypothyroidism. J Clin Endocrinol Metab. 2013 Apr;98(4):1403-8.
  • Evaluation of TSH cutoff value in blood-spot samples in neonatal screening for the diagnosis of congenital hypothyroidism in the Programa “Primeiros Passos” – IEDE/RJ]. Barone B, Lopes CL, Tyszler LS, do Amaral VB, Zarur RH, Paiva VN, Leite DB, Meirelles RM. Arq Bras Endocrinol Metabol. 2013 Feb;57(1):57-61.
  • De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say-Barber/Biesecker/Young-Simpson syndrome. Szakszon K, Salpietro C, Kakar N, Knegt AC, Oláh É, Dallapiccola B, Borck G. Am J Med Genet A. 2013 Apr;161(4):884-8.
  • Newborn screening for inborn errors of metabolism in mainland china: 30 years of experience. Shi XT, Cai J, Wang YY, Tu WJ, Wang WP, Gong LM, Wang DW, Ye YT, Fang SG, Jing PW. JIMD Rep. 2012;6:79-83.
  • Lymphatic edema in congenital disorders of glycosylation. Verstegen RH, Theodore M, van de Klerk H, Morava E. JIMD Rep. 2012;4:113-6.
  • Hypercortisolism and hypothyroidism in an infant with Smith-Lemli-Opitz syndrome. Kumar S, Suthar R, Panigrahi I. J Pediatr Endocrinol Metab. 2012;25(9-10):1001-5.
  • In congenital hypothyroidism, an initial L-thyroxine dose of 10-12 μg/kg/day is sufficient and sometimes excessive based on thyroid tests 1 month later. Vaidyanathan P, Pathak M, Kaplowitz PB. J Pediatr Endocrinol Metab. 2012;25(9-10):849-52.
  • Congenital hypothyroidism with eutopic thyroid gland: analysis of clinical and biochemical features at diagnosis and after re-evaluation. Rabbiosi S, Vigone MC, Cortinovis F, Zamproni I, Fugazzola L, Persani L, Corbetta C, Chiumello G, Weber G. J Clin Endocrinol Metab. 2013 Apr;98(4):1395-402
  • A novel mutation in thyrotropin (thyroid-stimulating hormone) gene in congenital hypothyroidism. Nirupam N, Maheshwari A, Gupta S, Aneja S, Seth A. J Pediatr Endocrinol Metab. 2013;26(5-6):565-7
  • The G395R Mutation of the Sodium/Iodide Symporter (NIS) Gene in Patients with Dyshormonogenetic Congenital Hypothyroidism. Mostofizade N, Nikpour P, Javanmard SH, Emadi-Baygi M, Miranzadeh-Mahabadi H, Hovsepian S, Hashemipour M. Int J Prev Med. 2013 Jan;4(1):57-62.
  • Langerhans cell histiocytosis case with dense metaphyseal band sign. Kikkawa I, Aihara T, Morimoto A, Watanabe H, Furukawa R. Pediatr Int. 2013 Feb;55(1):96-8.
  • Maternal hypothyroxinemia in early pregnancy predicts reduced performance in reaction time tests in 5- to 6-year-old offspring. Finken MJ, van Eijsden M, Loomans EM, Vrijkotte TG, Rotteveel J. J Clin Endocrinol Metab. 2013 Apr;98(4):1417-26.
  • The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance. Cassio A, Corbetta C, Antonozzi I, Calaciura F, Caruso U, Cesaretti G, Gastaldi R, Medda E, Mosca F, Pasquini E, Salerno MC, Stoppioni V, Tonacchera M, Weber G, Olivieri A; Italian Society for Pediatric Endocrinology and Diabetology; Italian Society for the Study of Metabolic Diseases and Neonatal Screening; Italian National Institute of Health; Italian National Coordinating Group for Congenital Hypothyroidism; Italian Thyroid Association; Italian Society of Pediatrics; Italian Society of Neonatology; Italian Society of Endocrinology; Associazione Medici Endocrinologi. J Endocrinol Invest. 2013 Mar;36(3):195-203
  • Genetic defects of hydrogen peroxide generation in the thyroid gland. Weber G, Rabbiosi S, Zamproni I, Fugazzola L. J Endocrinol Invest. 2013 Apr;36(4):261-6.
  • Congenital hypothyroidism after assisted reproductive technology in Japan: comparison between multiples and singletons, 2005-2009. Ooki S. Int J Pediatr Endocrinol. 2013 Feb 12;2013(1):5.
  • Perinatal and early infantile symptoms in congenital disorders of glycosylation. Funke S, Gardeitchik T, Kouwenberg D, Mohamed M, Wortmann SB, Korsch E, Adamowicz M, Al-Gazali L, Wevers RA, Horvath A, Lefeber DJ, Morava E. Am J Med Genet A. 2013 Mar;161(3):578-84.
  • Congenital hypothyroidism. Shanholtz HJ. J Pediatr Nurs. 2013 Apr;28(2):200-2. doi: 10.1016/j.pedn.2013.01.006
  • Vertical transmission of hypopituitarism: critical importance of appropriate interpretation of thyroid function tests and levothyroxine therapy during pregnancy. Pine-Twaddell E, Romero CJ, Radovick S. Thyroid. 2013 Jul;23(7):892-7.
  • Diagnosed congenital hypothyroidism with missing follow-up: is it time for a national registry? Al-Alwani I, AlRowaeah A, Bawazeer M. Ann Saudi Med. 2012 Nov-Dec;32(6):652-5.
  • Generic vs name brand L-thyroxine products: interchangeable or still not? Hennessey JV. J Clin Endocrinol Metab. 2013 Feb;98(2):511-4.
  • Health and disease in adults with Down syndrome. Malt EA, Dahl RC, Haugsand TM, Ulvestad IH, Emilsen NM, Hansen B, Cardenas YE, Skøld RO, Thorsen AT, Davidsen EM. Tidsskr Nor Laegeforen. 2013 Feb 5;133(3):290-4.
  • Identification and functional characterization of a novel mutation in the NKX2-1 gene: comparison with the data in the literature. Nettore IC, Mirra P, Ferrara AM, Sibilio A, Pagliara V, Kay CS, Lorenzoni PJ, Werneck LC, Bruck I, Dos Santos LH, Beguinot F, Salvatore D, Ungaro P, Fenzi G, Scola RH, Macchia PE. Thyroid. 2013 Jun;23(6):675-82.
  • The association between some endocrine disruptors in human plasma and the occurrence of congenital hypothyroidism. Jung H, Hong Y, Lee D, Pang K, Kim Y. Environ Toxicol Pharmacol. 2013 Mar;35(2):278-83.
  • Effects of early thyroid hormone deficiency on children’s autobiographical memory performance. Willoughby KA, McAndrews MP, Rovet J. J Int Neuropsychol Soc. 2013 Apr;19(4):419-29.
  • Endocrinology in 2012: what’s new?]. Parrat D, Meyer P. Rev Med Suisse. 2013 Jan 9;9(368):36-9.
  • All-cause and disease-specific mortality and morbidity in patients with congenital hypothyroidism treated since the neonatal period: a national population-based study. Azar-Kolakez A, Ecosse E, Dos Santos S, Léger J. J Clin Endocrinol Metab. 2013 Feb;98(2):785-93
  • 22q11.2 Microduplication with thyroid hemiagenesis. Kim HJ, Jo HS, Yoo EG, Chung IH, Kim SW, Lee KH, Chang YH. Horm Res Paediatr. 2013;79(4):243-9.
  • A novel mutation of IGSF1 in a Japanese patient of congenital central hypothyroidism without macroorchidism. Tajima T, Nakamura A, Ishizu K. Endocr J. 2013;60(2):245-9.
  • Fidelity of Administrative Data When Researching Down Syndrome. Jensen KM, Cooke CR, Davis MM. Med Care. 2013 Jan 25.
  • Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3. Jamsheer A, Sowińska A, Simon D, Jamsheer-Bratkowska M, Trzeciak T, Latos-Bieleńska A. BMC Med Genet. 2013 Jan 24;14:13.
  • Delivering Genetic Education and Genetic Counseling for Rare Diseases in Rural Brazil. Acosta AX, Abé-Sandes K, Giugliani R, Bittles AH. J Genet Couns. 2013 Jan 22
  • Hospitalizations and mortality in the United States for adults with Down syndrome and congenital heart disease. Baraona F, Gurvitz M, Landzberg MJ, Opotowsky AR. Am J Cardiol. 2013 Apr 1;111(7):1046-51.
  • Neonatal screening for congenital hypothyroidism in Japan. Minamitani K, Inomata H. Pediatr Endocrinol Rev. 2012 Oct;10 Suppl 1:79-88.
  • Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation. Baş VN, Cangul H, Agladioglu SY, Kendall M, Cetinkaya S, Maher ER, Aycan Z. J Pediatr Endocrinol Metab. 2012;25(11-12):1153-6.
  • Newborn Screening Program for congenital hypothyroidism of the State of Santa Catarina, Brazil: etiological investigation in the first visit].Nascimento ML, Rabello FH, Ohira M, Simoni G, Cechinel E, Linhares RM, da Silva PC. Arq Bras Endocrinol Metabol. 2012 Dec;56(9):627-32.
  • Mutations of the thyroid peroxidase gene in Chinese siblings with congenital goitrous hypothyroidism. Ma SG, Wu XJ, Liu H, Xu W, He L. Arq Bras Endocrinol Metabol. 2012 Dec;56(9):614-7.
  • Maternal marginal iodine deficiency affects the expression of relative proteins during brain development in rat offspring. Liu Y, Zhang L, Li J, Shan Z, Teng W. J Endocrinol. 2013 Mar 15;217(1):21-9.
  • High prevalence of congenital hypothyroidism in Isfahan: Do familial components have a role? Hashemipour M, Hovsepian S, Kelishadi R. Adv Biomed Res. 2012;1:37
  • Comparison between liquid and tablet formulations of levothyroxine in the initial treatment of congenital hypothyroidism. Cassio A, Monti S, Rizzello A, Bettocchi I, Baronio F, D’Addabbo G, Bal MO, Balsamo A. J Pediatr. 2013 Jun;162(6):1264-9, 1269.e1-2
  • The characteristics of lipid metabolism in children with congenital hypothyroidism against the background of substitutive therapy with L-thyroxin]. Romankova TM, Alimova IL, Sukhorukov VS. Klin Lab Diagn. 2012 Nov;(11):18-20.
  • Community genetic services in iran. Atri Barzanjeh S, Behshid M, Hosseini MB, Ezari M, Taghizadeh M, Dastgiri S. Genet Res Int. 2012;2012:129575.
  • Transient neonatal hypothyroidism in a boy with unbalanced translocation t(8;16). Secchi LA, Mazzeu JF, Córdoba MS, Ferrari I, Ramos HE, Neves Fde A. Arq Bras Endocrinol Metabol. 2012 Nov;56(8):564-9.
  • Generic levothyroxine compared with synthroid in young children with congenital hypothyroidism. Lomenick JP, Wang L, Ampah SB, Saville BR, Greenwald FI. J Clin Endocrinol Metab. 2013 Feb;98(2):653-8
  • Congenital hypothyroidism: a review of the risk factors. Dalili S, Rezvany SM, Dadashi A, Medghalchi A, Mohammadi H, Dalili H, Mirzanejad M, Gholamnezhad H, Amirhakimi A. Acta Med Iran. 2012 Nov;50(11):735-9.
  • A novel dual oxidase maturation factor 2 gene mutation for congenital hypothyroidism. Yi RH, Zhu WB, Yang LY, Lan L, Chen Y, Zhou JF, Wang J, Su YQ. Int J Mol Med. 2013 Feb;31(2):467-70.
  • Epidemiology and clinical characteristics of congenital hypothyroidism in an Asian population: a nationwide population-based study. Chen CY, Lee KT, Lee CT, Lai WT, Huang YB. J Epidemiol. 2013;23(2):85-94.
  • Generic and brand-name L-thyroxine are not bioequivalent for children with severe congenital hypothyroidism. Carswell JM, Gordon JH, Popovsky E, Hale A, Brown RS. J Clin Endocrinol Metab. 2013 Feb;98(2):610-7
  • Different aspects of kidney function in well-controlled congenital hypothyroidism. Gheissari A, Hashemipour M, Khosravi P, Adibi A. J Clin Res Pediatr Endocrinol. 2012 Dec;4(4):193-8.
  • Prediction of adult height by Tanner-Whitehouse method in young Caucasian male athletes. Ostojic SM. QJM. 2013 Apr;106(4):341-5.
  • Delayed onset congenital hypothyroidism in a patient with DUOX2 mutations and maternal iodine excess. Kasahara T, Narumi S, Okasora K, Takaya R, Tamai H, Hasegawa T. Am J Med Genet A. 2013 Jan;161A(1):214-7.
  • Weaver syndrome and defective cortical development: a rare association. Al-Salem A, Alshammari MJ, Hassan H, Alazami AM, Alkuraya FS. Am J Med Genet A. 2013 Jan;161A(1):225-7
  • Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community. Cangul H, Aycan Z, Olivera-Nappa A, Saglam H, Schoenmakers NA, Boelaert K, Cetinkaya S, Tarim O, Bober E, Darendeliler F, Bas V, Demir K, Aydin BK, Kendall M, Cole T, Högler W, Chatterjee VK, Barrett TG, Maher ER. Clin Endocrinol (Oxf). 2013 Aug;79(2):275-81.
  • Kocher-Debre-Semelaigne syndrome with arrhythmogenic right ventricular cardiomyopathy: A hitherto unrecognized association. Moorthy N, Kumar S, Dabadghao P, Kapoor A. Indian J Endocrinol Metab. 2012 Nov;16(6):1032-4.
  • A thyroid peroxidase (TPO) mutation in dogs reveals a canid-specific gene structure. Fyfe JC, Lynch M, Olsen J, Louёr E. Mamm Genome. 2013 Apr;24(3-4):127-33
  • Thyroid dysfunction in pregnant women: clinical dilemmas]. Vissenberg R, Goddijn M, Mol BW, van der Post JA, Fliers E, Bisschop PH. Ned Tijdschr Geneeskd. 2012;156(49):A5163.
  • Congenital adenohypophyseal hypoplasia associated with secondary hypothyroidism in a 2-week-old Portuguese water dog. Gal A, Raetzman LT, Singh K. Can Vet J. 2012 Jun;53(6):659-64.
  • Incidence and characteristics of pseudoprecocious puberty because of severe primary hypothyroidism. Cabrera SM, DiMeglio LA, Eugster EA. J Pediatr. 2013 Mar;162(3):637-9.
  • Refractory cardiogenic shock in an infant with congenital hypothyroidism. Zaki SA, Dolas A. Indian J Crit Care Med. 2012 Jul;16(3):151-3.
  • Screening for congenital hypothyroidism in newborns transferred to neonatal intensive care. Korzeniewski SJ, Kleyn M, Young WI, Chaiworapongsa T, Schwartz AG, Romero R. Arch Dis Child Fetal Neonatal Ed. 2013 Jul;98(4):F310-5.
  • Congenital von Willebrand’s disease and clinical hypothyroidism. Hassan S, Qureshi W, Donthireddy V, Kuriakose P. Haemophilia. 2013 Mar;19(2):242-5.
  • Choreoathetosis, congenital hypothyroidism and neonatal respiratory distress syndrome with intact NKX2-1. Barnett CP, Mencel JJ, Gecz J, Waters W, Kirwin SM, Vinette KM, Uppill M, Nicholl J. Am J Med Genet A. 2012 Dec;158A(12):3168-73.
  • New insights into thyroglobulin gene: molecular analysis of seven novel mutations associated with goiter and hypothyroidism. Citterio CE, Machiavelli GA, Miras MB, Gruñeiro-Papendieck L, Lachlan K, Sobrero G, Chiesa A, Walker J, Muñoz L, Testa G, Belforte FS, González-Sarmiento R, Rivolta CM, Targovnik HM. Mol Cell Endocrinol. 2013 Jan 30;365(2):277-91.

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PICKY EATERS AND GROW UP CLINIC (Klinik Khusus Kesulitan Makan dan Gangguan Berat Badan) GRoW UP CLINIC JAKARTAYudhasmara Foundation Inspirasi Orangtua Cerdas, Tumbuhkan Anak Semakin Sehat, Kuat dan Pintar

WORKING TOGETHER SUPPORT TO THE HEALTH OF ALL BY CLINICAL, RESEARCH AND EDUCATIONS. Advancing of the future pediatric and future parenting to optimalized physical, mental and social health and well being for fetal, newborn, infant, children, adolescents and young adult
“GRoW UP CLINIC JAKARTA” For Children, Teen and Adult Focus and Interest on:

Professional Healthcare Provider “GRoW UP CLINIC”

  • Dr Narulita Dewi SpKFR, Physical Medicine & Rehabilitation curriculum vitae HP 085777227790 PIN BB 235CF967
  • Dr Widodo Judarwanto, Pediatrician
  • Fisioterapis dan terapi okupasi lainnya

Clinical – Editor in Chief :

Dr WIDODO JUDARWANTO, pediatrician

Information on this web site is provided for informational purposes only and is not a substitute for professional medical advice. You should not use the information on this web site for diagnosing or treating a medical or health condition. You should carefully read all product packaging. If you have or suspect you have a medical problem, promptly contact your professional healthcare provider

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