-
1
-
-
0023860052
-
Iodine in contrast agents and skin disinfectants is the major cause for hypothyroidism in premature infants during intensive care
-
l'Allemand D, Grüters A, Beyer P, Weber: Iodine in contrast agents and skin disinfectants is the major cause for hypothyroidism in premature infants during intensive care. Hormon Res. 28: 42-49, 1987
-
(1987)
Hormon Res.
, vol.28
, pp. 42-49
-
-
L'Allemand, D.1
Grüters, A.2
Beyer, P.3
Weber4
-
2
-
-
0031012235
-
Transient iodine organification defect in infants with ectopic thyroid glands
-
al-Jurayyan NA, el-Desouki-MI: Transient iodine organification defect in infants with ectopic thyroid glands. Clin-Nucl-Med. 22: 13-6, 1997
-
(1997)
Clin-Nucl-Med.
, vol.22
, pp. 13-16
-
-
Al-Jurayyan, N.A.1
El-Desouki, M.I.2
-
3
-
-
0027618636
-
Newbornscreening for congenital hypothyroidism: Recommended guidelines
-
American Academy of Pediatrics AAP Section on Endocrinology and Committee on Genetics, and American Thyroid AssociationCommittee on Public Health: Newbornscreening for congenital hypothyroidism: recommended guidelines. Pediatrics. 91: 1203-9, 1993
-
(1993)
Pediatrics
, vol.91
, pp. 1203-1209
-
-
-
4
-
-
0031025824
-
Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects
-
Bikker H, Baas F, De Vijlder JJ: Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects. J Clin-Endocrinol-Metab. 82: 694-53, 1997
-
(1997)
J Clin-Endocrinol-Metab.
, vol.82
, pp. 694-753
-
-
Bikker, H.1
Baas, F.2
De Vijlder, J.J.3
-
5
-
-
0002395057
-
Iodine deficiency, implications for mental and psychomotor development in children
-
DeLong GR, Robbins J, Condliffe PG (eds): Plenum New York
-
Bleichrodt N, Escobar del Rey F, Morreale de Escobar G, Garcia I, Rubio C: Iodine deficiency, implications for mental and psychomotor development in children. In: DeLong GR, Robbins J, Condliffe PG (eds): Iodine and the brain, pp. 269-287, Plenum New York, 1989
-
(1989)
Iodine and the Brain
, pp. 269-287
-
-
Bleichrodt, N.1
Escobar Del Rey, F.2
Morreale De Escobar, G.3
Garcia, I.4
Rubio, C.5
-
6
-
-
0024604830
-
Cytotoxic antibodies in congenital hypothyroidism
-
Bogner U, Grüters A, Sigle B, Helge H, Schleusener H: Cytotoxic antibodies in congenital hypothyroidism. J.Clin Endocrinol Metab 68:671, 1989
-
(1989)
J.Clin Endocrinol Metab
, vol.68
, pp. 671
-
-
Bogner, U.1
Grüters, A.2
Sigle, B.3
Helge, H.4
Schleusener, H.5
-
7
-
-
0029863763
-
Incidence of transient congenital hypothyroidism due to maternal thyrotropin receptor-blocking antibodies in over one million babies
-
Brown RS, Bellisario RL, Botero D, Fournier L, Abrams CA, Cowger ML, David R, Fort P, Richman RA: Incidence of transient congenital hypothyroidism due to maternal thyrotropin receptor-blocking antibodies in over one million babies. J-Clin-Endocrinol-Metab. 81(3): 1147-51, 1996
-
(1996)
J-Clin-Endocrinol-Metab.
, vol.81
, Issue.3
, pp. 1147-1151
-
-
Brown, R.S.1
Bellisario, R.L.2
Botero, D.3
Fournier, L.4
Abrams, C.A.5
Cowger, M.L.6
David, R.7
Fort, P.8
Richman, R.A.9
-
8
-
-
0030797640
-
Routine skin cleansing with povidone-iodine is not a common cause of transient neonatal hypothyroidism in North America: A prospective controlled study
-
Brown RS, Bloomfield S, Bednarek FJ, Mitchell M, Braverman LE: Routine skin cleansing with povidone-iodine is not a common cause of transient neonatal hypothyroidism in North America: A prospective controlled study. Thyroid 7: 395-400, 1997
-
(1997)
Thyroid
, vol.7
, pp. 395-400
-
-
Brown, R.S.1
Bloomfield, S.2
Bednarek, F.J.3
Mitchell, M.4
Braverman, L.E.5
-
9
-
-
0002056995
-
Neurologic involvement in iodine deficiency disorders
-
Hetzel et al. eds.: Elsevien Amsterdam
-
Delong R: Neurologic involvement in iodine deficiency disorders. In Hetzel et al. eds.: The prevention and control of iodine deficienc disorders pp. 49-63, Elsevien Amsterdam, 1987
-
(1987)
The Prevention and Control of Iodine Deficienc Disorders
, pp. 49-63
-
-
Delong, R.1
-
10
-
-
0030029503
-
Neuropsychologie development in early treated congenital hypothyroidism: Analysis of literaure data
-
Derksen-Lubsen G, Verkerk PH: Neuropsychologie development in early treated congenital hypothyroidism: analysis of literaure data. Pediatr-Res. 39: 561-6, 1996
-
(1996)
Pediatr-Res.
, vol.39
, pp. 561-566
-
-
Derksen-Lubsen, G.1
Verkerk, P.H.2
-
11
-
-
0029099658
-
Thyroid scintigraphy and perchlorate dischargetest in the diagnosis of congenital hypothyroidism
-
el-Desouki M, al-Jurayyan N, al Muaim A, al-Herbish A, Abo-Bakr A, al-Mazrou Y, al-Swailem A: Thyroid scintigraphy and perchlorate dischargetest in the diagnosis of congenital hypothyroidism (see comments). Eur-J-Nucl-Med. 22: 1005-8, 1995
-
(1995)
Eur-J-Nucl-Med.
, vol.22
, pp. 1005-1008
-
-
El-Desouki, M.1
Al-Jurayyan, N.2
Al Muaim, A.3
Al-Herbish, A.4
Abo-Bakr, A.5
Al-Mazrou, Y.6
Al-Swailem, A.7
-
12
-
-
0028293556
-
Guidelines for neonatal screening programs for congenital hypothyroidism
-
European Society for Pediatric Endocrinology Working Group on Congenital Hypothyroidism (Grüters A et al): Guidelines for neonatal screening programs for congenital hypothyroidism. Horm-Res. 41(1): 1-2, 1994
-
(1994)
Horm-Res.
, vol.41
, Issue.1
, pp. 1-2
-
-
Grüters, A.1
-
13
-
-
0022562233
-
Thyroid disorders - Possible role of environmental pollutants and naturally occurring agents
-
Gaitan E: Thyroid disorders - possible role of environmental pollutants and naturally occurring agents. Am. Chem. Soc., Div. Environ. Chem. 26: 58-66,1986
-
(1986)
Am. Chem. Soc., Div. Environ. Chem.
, vol.26
, pp. 58-66
-
-
Gaitan, E.1
-
14
-
-
0000091215
-
Richtlinien zur Organisation und Durchführung des Neugeborenenscreenings auf angeborene Stoffwechselstörungen und Endokrinopathien in Deutschland
-
German expert committee on neonatal screening (Harms et al.): Richtlinien zur Organisation und Durchführung des Neugeborenenscreenings auf angeborene Stoffwechselstörungen und Endokrinopathien in Deutschland. Monatsschr. Kinderheilkd 145: 770-772, 1997
-
(1997)
Monatsschr. Kinderheilkd
, vol.145
, pp. 770-772
-
-
Harms1
-
15
-
-
0026688210
-
Intellectual development at age 12 years of children with congenital hypothyroidism diagnosed by neonatal screening
-
Glorieux J, Dussault J, Van-Vliet G: Intellectual development at age 12 years of children with congenital hypothyroidism diagnosed by neonatal screening. J-Pediatr. 121: 581-4, 1992
-
(1992)
J-Pediatr.
, vol.121
, pp. 581-584
-
-
Glorieux, J.1
Dussault, J.2
Van-Vliet, G.3
-
16
-
-
0027918035
-
Jodmangel in der Bundesrepublik Deutschland
-
Gutekunst, R, U. Magiera, H.M. Teichert: Jodmangel in der Bundesrepublik Deutschland. Med. Klin. 88: 525-528, 1993.
-
(1993)
Med. Klin.
, vol.88
, pp. 525-528
-
-
Gutekunst, R.1
Magiera, U.2
Teichert, H.M.3
-
17
-
-
0028266582
-
Etiological grouping of permanent congenital hypothyroidism with a thyroid gland in situ
-
Grüters A, Finke R, Krude H, Meinhold H: Etiological grouping of permanent congenital hypothyroidism with a thyroid gland in situ Horm-Res. 1994; 41(1): 3-9
-
(1994)
Horm-Res.
, vol.41
, Issue.1
, pp. 3-9
-
-
Grüters, A.1
Finke, R.2
Krude, H.3
Meinhold, H.4
-
18
-
-
0029855448
-
Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism
-
Grüters A, Kohler B, Wolf A, de Vijlder L, Krude H, Biebermann H.: Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism. Exp-Clin-Endocrinol-Diabetes, 104 Suppl. 4: 121-3, 1996
-
(1996)
Exp-Clin-Endocrinol-Diabetes
, vol.104
, Issue.4 SUPPL.
, pp. 121-123
-
-
Grüters, A.1
Kohler, B.2
Wolf, A.3
De Vijlder, L.4
Krude, H.5
Biebermann, H.6
-
20
-
-
9044226533
-
Defective organification of iodide causing congenital goitrous hypothyroidism
-
Ishikawa N, Eguchi K, Ohomori T, Momotani N, Nagayama Y, Hosoya Y, Oguchi H, Mimura T, Kimura S, Nagataki S, Ito K: Defective organification of iodide causing congenital goitrous hypothyroidism. J-Clin-Endocrinol-Metab. 81: 376-83, 1996
-
(1996)
J-Clin-Endocrinol-Metab.
, vol.81
, pp. 376-383
-
-
Ishikawa, N.1
Eguchi, K.2
Ohomori, T.3
Momotani, N.4
Nagayama, Y.5
Hosoya, Y.6
Oguchi, H.7
Mimura, T.8
Kimura, S.9
Nagataki, S.10
Ito, K.11
-
21
-
-
12644283550
-
Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequuent cause of congenital hypothyroidism with thyroid dysgenesis
-
Lapi P, Macchia PE, Chiovato L, Bifall E, Moshini L, Larizza D, Baserga M, Pinchera A, Fenzi G, Di Lauro R: Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequuent cause of congenital hypothyroidism with thyroid dysgenesis. Thyroid 7: 383-387, 1997
-
(1997)
Thyroid
, vol.7
, pp. 383-387
-
-
Lapi, P.1
Macchia, P.E.2
Chiovato, L.3
Bifall, E.4
Moshini, L.5
Larizza, D.6
Baserga, M.7
Pinchera, A.8
Fenzi, G.9
Di Lauro, R.10
-
22
-
-
0026904349
-
Birth prevalence of primary congenital hypothyroidism by sex and ethnicity
-
Lorey FW, Cunningham GC: Birth prevalence of primary congenital hypothyroidism by sex and ethnicity. Hum-Biol. 64: 531-8, 1992
-
(1992)
Hum-Biol.
, vol.64
, pp. 531-538
-
-
Lorey, F.W.1
Cunningham, G.C.2
-
23
-
-
0030481624
-
Congenital hypothyroid goiter with deficient thyroglobulin. Indentification of an endoplasmic reticulum storage disease with induction of molecular chaperones
-
Medeiros-Neto G, Kum PS, Yoo SE, Vono J, Targovnik HM, Camargo R, Hossain SA, Arvan P: Congenital hypothyroid goiter with deficient thyroglobulin. Indentification of an endoplasmic reticulum storage disease with induction of molecular chaperones. J-Clin-Invest. 98: 2838-44, 1996
-
(1996)
J-Clin-Invest.
, vol.98
, pp. 2838-2844
-
-
Medeiros-Neto, G.1
Kum, P.S.2
Yoo, S.E.3
Vono, J.4
Targovnik, H.M.5
Camargo, R.6
Hossain, S.A.7
Arvan, P.8
-
24
-
-
0028398934
-
The screening programme for congenital hypothyroidism in Greece: Evidence of iodine deficiency in some areas of the country
-
Mengreli C, Yiannakou L, Pantelakis S.:The screening programme for congenital hypothyroidism in Greece: evidence of iodine deficiency in some areas of the country. Acta Paediatr. Suppl. 394: 47-51, 1994
-
(1994)
Acta Paediatr. Suppl.
, vol.394
, pp. 47-51
-
-
Mengreli, C.1
Yiannakou, L.2
Pantelakis, S.3
-
25
-
-
0028296942
-
Correlation of cognitive test scores and adequacy of treatment in adolescents with congenital hypothyroidism
-
New England Congenital Hypothyroidism Collaborative: Correlation of cognitive test scores and adequacy of treatment in adolescents with congenital hypothyroidism. J. Pediatr 124: 383-387, 1994
-
(1994)
J. Pediatr
, vol.124
, pp. 383-387
-
-
-
26
-
-
0029081181
-
Outcome in three siblings with antibody-mediated transient congenial hypothyroidism
-
Pacaud D, Huot C, Gattereau A, Brown RS, Glorieux J, Dussault JH, Van-Vliet G: Outcome in three siblings with antibody-mediated transient congenial hypothyroidism. J-Pediatr. 127: 275-7, 1995
-
(1995)
J-Pediatr.
, vol.127
, pp. 275-277
-
-
Pacaud, D.1
Huot, C.2
Gattereau, A.3
Brown, R.S.4
Glorieux, J.5
Dussault, J.H.6
Van-Vliet, G.7
-
27
-
-
0029844539
-
Iodine, Thyroid function and very low birth weight infants
-
Parravicini E, Fontana C, Paterlini G, Tagliabue P, Rovelli F, Leung K, Stark RI,: Iodine, Thyroid function and very low birth weight infants. Pediatrics 98: 730-734, 1996
-
(1996)
Pediatrics
, vol.98
, pp. 730-734
-
-
Parravicini, E.1
Fontana, C.2
Paterlini, G.3
Tagliabue, P.4
Rovelli, F.5
Leung, K.6
Stark, R.I.7
-
28
-
-
0030839127
-
Absence of mutations in the gene encoding thyroid transcription factor-1 (TTF-1) in patients with thyroid dysgenesis
-
Perna MG, Civitareale D, De Filippis, V., Sacco M, Cisternino C, Tassi V: Absence of mutations in the gene encoding thyroid transcription factor-1 (TTF-1) in patients with thyroid dysgenesis. Thyroid 7: 377-381, 1997
-
(1997)
Thyroid
, vol.7
, pp. 377-381
-
-
Perna, M.G.1
Civitareale, D.2
De Filippis, V.3
Sacco, M.4
Cisternino, C.5
Tassi, V.6
-
29
-
-
0031579264
-
Correlates of low thyroxine values at newborn screening among infants born before 32 weeks gestation
-
Reuss ML, Paneth N, Lorenz JM, Susser M: Correlates of low thyroxine values at newborn screening among infants born before 32 weeks gestation, Early-Hum-Dev. 47: 223-33, 1997
-
(1997)
Early-Hum-Dev.
, vol.47
, pp. 223-233
-
-
Reuss, M.L.1
Paneth, N.2
Lorenz, J.M.3
Susser, M.4
-
30
-
-
0030034535
-
Low thyroxinaemia occurs m the majority of very preterm newborns
-
Rooman RP, Du-Caju MV, De-Beek LO, Docx M, Van Reempts P, Van-Acker KJ: Low thyroxinaemia occurs m the majority of very preterm newborns. Eur-J-Pediatr. 155: 211-5, 1996
-
(1996)
Eur-J-Pediatr.
, vol.155
, pp. 211-215
-
-
Rooman, R.P.1
Du-Caju, M.V.2
De-Beek, L.O.3
Docx, M.4
Van Reempts, P.5
Van-Acker, K.J.6
-
31
-
-
0027862618
-
Thyroid dysfunction in newborns and infants living in an iodine-deficient area
-
Rybakowa M, Ratajczak R, Tylek D: Thyroid dysfunction in newborns and infants living in an iodine-deficient area. Folia Med-Cracow 34: 59-63, 1993
-
(1993)
Folia Med-Cracow
, vol.34
, pp. 59-63
-
-
Rybakowa, M.1
Ratajczak, R.2
Tylek, D.3
-
32
-
-
0027338391
-
Maternal-fetal T4 transfer does not suffice to prevent the effects of in utero hypothyroidism
-
Sack J, Kaisermann I, Siebner R:Maternal-fetal T4 transfer does not suffice to prevent the effects of in utero hypothyroidism. Horm-Res. 39: 1-7, 1993
-
(1993)
Horm-Res.
, vol.39
, pp. 1-7
-
-
Sack, J.1
Kaisermann, I.2
Siebner, R.3
-
33
-
-
0029993005
-
Thyroid screening for early discharged infants
-
Saslow JG, Post EM, Southard CA: Thyroid screening for early discharged infants. Pediatrics 98: 41-4, 1996
-
(1996)
Pediatrics
, vol.98
, pp. 41-44
-
-
Saslow, J.G.1
Post, E.M.2
Southard, C.A.3
-
34
-
-
84889523295
-
Datenerhebung für das Jahr 1996
-
Deutsche Gesellschaft für Neugeborenenscreening (DGNS), Datenerhebung für das Jahr 1996, Screening Journal 2: 6-13, 1997
-
(1997)
Screening Journal
, vol.2
, pp. 6-13
-
-
-
35
-
-
0028060229
-
Intellectual development at 10 years in early treated congenital hypothyroidism
-
Simons WF, Fuggle PW, Grant DB, Smith I: Intellectual development at 10 years in early treated congenital hypothyroidism. Arch Dis Childh 71: 232-234, 1994
-
(1994)
Arch Dis Childh
, vol.71
, pp. 232-234
-
-
Simons, W.F.1
Fuggle, P.W.2
Grant, D.B.3
Smith, I.4
-
36
-
-
0028708550
-
Neonatal screening in congenital hypothyroidism in Italy. The National Registry
-
Sorcini A, Fazzini C, Olivieri A Grandolfo ME, Medda E, Stazi MA, Balestrazzi P, Giovannelli G, Cara S: (Neonatal screening in congenital hypothyroidism in Italy. The National Registry). Ann-Ist-Super-Sanita. 30: 275-87, 1994
-
(1994)
Ann-Ist-Super-Sanita
, vol.30
, pp. 275-287
-
-
Sorcini, A.1
Fazzini, C.2
Olivieri, A.3
Grandolfo, M.E.4
Medda, E.5
Stazi, M.A.6
Balestrazzi, P.7
Giovannelli, G.8
Cara, S.9
-
37
-
-
0027144992
-
Familial unresponsiveness to thyrotropin by autosomal recessive inheritance
-
Takamatsu J, Nishikawa M, Horimoto M, Ohsawa N: Familial unresponsiveness to thyrotropin by autosomal recessive inheritance. J-Clin-Endocrinol-Metab.: 77: 1569-73, 1993
-
(1993)
J-Clin-Endocrinol-Metab.
, vol.77
, pp. 1569-1573
-
-
Takamatsu, J.1
Nishikawa, M.2
Horimoto, M.3
Ohsawa, N.4
-
38
-
-
0026968920
-
Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world
-
Toublanc JE: Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world. Horm-Res. 38: 230-5, 1992
-
(1992)
Horm-Res.
, vol.38
, pp. 230-235
-
-
Toublanc, J.E.1
-
39
-
-
0029302847
-
Prevalence of permanent primary congenital hypothyroidism in Taiwan
-
Tsai WY, Lee JS, Chao MC, Chen LY, Lin SJ, Wu KH, Wang TR, Chen JS, Chuang SM: Prevalence of permanent primary congenital hypothyroidism in Taiwan. J-Formos-Med-Assoc. 94: 271-3, 1995
-
(1995)
J-Formos-Med-Assoc.
, vol.94
, pp. 271-273
-
-
Tsai, W.Y.1
Lee, J.S.2
Chao, M.C.3
Chen, L.Y.4
Lin, S.J.5
Wu, K.H.6
Wang, T.R.7
Chen, J.S.8
Chuang, S.M.9
-
40
-
-
84889529548
-
Molecular genetics and pathology of the TSH-receptor
-
Vassart G: Molecular genetics and pathology of the TSH-receptor. Thyroid 7: 501-502, 1997
-
(1997)
Thyroid
, vol.7
, pp. 501-502
-
-
Vassart, G.1
-
41
-
-
0027673716
-
Körperliche und geistige Entwicklung von Kindern mit konnataler Hypothyreose
-
Winkler L, Bank S, Bremer-Hübler U, Brodehl J, Sander J: Körperliche und geistige Entwicklung von Kindern mit konnataler Hypothyreose. Monatsschr Kinderheilkd 141: 799-804, 1993
-
(1993)
Monatsschr Kinderheilkd
, vol.141
, pp. 799-804
-
-
Winkler, L.1
Bank, S.2
Bremer-Hübler, U.3
Brodehl, J.4
Sander, J.5
-
42
-
-
0029096084
-
Screening for congenital hypothyroidism in Turkey
-
Yordam H Calikoglu AS, Hatun S, Kandemir N, Oguz H, Tezic T, Ozalp I: Screening for congenital hypothyroidism in Turkey. Eur. J. Pediatr. 154: 614-6, 1995
-
(1995)
Eur. J. Pediatr.
, vol.154
, pp. 614-616
-
-
Yordam, H.1
Calikoglu, A.S.2
Hatun, S.3
Kandemir, N.4
Oguz, H.5
Tezic, T.6
Ozalp, I.7
-
43
-
-
0029312223
-
Classification of congenital hypothyroidism bases on scintigraphy, ultrasonography and the serum thyroglobulin level
-
Yoshimura R, Kodama S, Nakamura H: Classification of congenital hypothyroidism bases on scintigraphy, ultrasonography and the serum thyroglobulin level Kobe-J-Med-Sci. 41: 71-82, 1995
-
(1995)
Kobe-J-Med-Sci.
, vol.41
, pp. 71-82
-
-
Yoshimura, R.1
Kodama, S.2
Nakamura, H.3
-
44
-
-
0027567770
-
Experience in neonatal screening for congenital hypothyroidism
-
Zhang YQ, Cao QX: Experience in neonatal screening for congenital hypothyroidism. Chin-Med-J-Engl. 106: 216-9, 1993
-
(1993)
Chin-Med-J-Engl.
, vol.106
, pp. 216-219
-
-
Zhang, Y.Q.1
Cao, Q.X.2
|