-
1
-
-
0033454741
-
Guidelines for neonatal screening programs for congenital hypothyroidism
-
Working Group for Neonatal Screening in Paediatric Endocrinology of the European Society for Paediatric Endocrinology
-
Toublanc JE. Guidelines for neonatal screening programs for congenital hypothyroidism. Working Group for Neonatal Screening in Paediatric Endocrinology of the European Society for Paediatric Endocrinology. Acta Paediatrica 1999 88 (Suppl.) 13-14.
-
(1999)
Acta Paediatrica
, vol.88
, Issue.SUPPL.
, pp. 13-14
-
-
Toublanc, J.E.1
-
3
-
-
0027517385
-
The National Register of Infants with Congenital Hypothyroidism detected by neonatal screening in Italy
-
Sorcini M, Balestrazzi P, Grandolfo ME, Carta S & Giovannelli G. The National Register of Infants with Congenital Hypothyroidism detected by neonatal screening in Italy. Journal of Endocrinological Investigation 1993 16 573-577.
-
(1993)
Journal of Endocrinological Investigation
, vol.16
, pp. 573-577
-
-
Sorcini, M.1
Balestrazzi, P.2
Grandolfo, M.E.3
Carta, S.4
Giovannelli, G.5
-
4
-
-
0041328169
-
An outline of inherited disorders of the thyroid hormone generating system
-
Knobel M & Medeiros-Neto G. An outline of inherited disorders of the thyroid hormone generating system. Thyroid 2003 13 771-801.
-
(2003)
Thyroid
, vol.13
, pp. 771-801
-
-
Knobel, M.1
Medeiros-Neto, G.2
-
5
-
-
0042632714
-
Development of the thyroid gland: Lessons from congenitally hypothyroid mice and men
-
Van Vliet G. Development of the thyroid gland: lessons from congenitally hypothyroid mice and men. Clinical Genetics 2003 63 445-455.
-
(2003)
Clinical Genetics
, vol.63
, pp. 445-455
-
-
Van Vliet, G.1
-
6
-
-
0036093069
-
Perspective: Genetic defects in the etiology of congenital hypothyroidism
-
Kopp P. Perspective: genetic defects in the etiology of congenital hypothyroidism. Endocrinology 2002 143 2019-2024.
-
(2002)
Endocrinology
, vol.143
, pp. 2019-2024
-
-
Kopp, P.1
-
7
-
-
6444245853
-
Genetics of specific phenotypes of congenital hypothyroidism: A population-based approach
-
Calaciura F, Miscio G, Coco A, Leonardi D, Cisternino C, Regalbuto C, Bozzali M, Maiorana R, Ranieri A, Carta A, Buscema M, Trischitta V, Sava L & Tassi V. Genetics of specific phenotypes of congenital hypothyroidism: a population-based approach. Thyroid 2002 12 945-951.
-
(2002)
Thyroid
, vol.12
, pp. 945-951
-
-
Calaciura, F.1
Miscio, G.2
Coco, A.3
Leonardi, D.4
Cisternino, C.5
Regalbuto, C.6
Bozzali, M.7
Maiorana, R.8
Ranieri, A.9
Carta, A.10
Buscema, M.11
Trischitta, V.12
Sava, L.13
Tassi, V.14
-
8
-
-
0037341985
-
The W546X mutation of the thyrotropin receptor gene: Potential major contributor to thyroid dysfunction in a Caucasian population
-
Jordan N, Williams N, Gregory JW, Evans C, Owen M & Ludgate M. The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian population. Journal of Clinical Endocrinology and Metabolism 2003 88 1002-1005.
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, pp. 1002-1005
-
-
Jordan, N.1
Williams, N.2
Gregory, J.W.3
Evans, C.4
Owen, M.5
Ludgate, M.6
-
9
-
-
1042288131
-
Congenital hypothyroidism and apparent athyreosis with compound heterozygosity or compensated hypothyroidism with probable hemizygosity for inactivating mutations of the TSH receptor
-
Park SM, Clifton-Bligh RJ, Betts P & Chatterjee VK. Congenital hypothyroidism and apparent athyreosis with compound heterozygosity or compensated hypothyroidism with probable hemizygosity for inactivating mutations of the TSH receptor. Clinical Endocrinology 2004 60 220-227.
-
(2004)
Clinical Endocrinology
, vol.60
, pp. 220-227
-
-
Park, S.M.1
Clifton-Bligh, R.J.2
Betts, P.3
Chatterjee, V.K.4
-
10
-
-
4544229648
-
Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid
-
Meeus L, Gilbert B, Rydlewski C, Parma J, Roussie AL, Abramowicz M, Vilain C, Christophe D, Costagliola S & Vassart G. Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid. Journal of Clinical Endocrinology and Metabolism 2004 89 4285-4291.
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, pp. 4285-4291
-
-
Meeus, L.1
Gilbert, B.2
Rydlewski, C.3
Parma, J.4
Roussie, A.L.5
Abramowicz, M.6
Vilain, C.7
Christophe, D.8
Costagliola, S.9
Vassart, G.10
-
11
-
-
0036231997
-
Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism
-
Umeki K, Kotani T, Kawano J, Suganuma T, Yamamoto I, Aratake Y, Furujo M & Ichiba Y. Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism. European Journal of Endocrinology 2002 146 491-498.
-
(2002)
European Journal of Endocrinology
, vol.146
, pp. 491-498
-
-
Umeki, K.1
Kotani, T.2
Kawano, J.3
Suganuma, T.4
Yamamoto, I.5
Aratake, Y.6
Furujo, M.7
Ichiba, Y.8
-
12
-
-
0037961011
-
Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect
-
Fugazzola L, Cerutti N, Mannavola D, Vannucchi G, Fallini C, Persani L & Beck-Peccoz P. Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect. Journal of Clinical Endocrinology and Metabolism 2003 88 3264-3271.
-
(2003)
Journal of Clinical Endocrinology and Metabolism
, vol.88
, pp. 3264-3271
-
-
Fugazzola, L.1
Cerutti, N.2
Mannavola, D.3
Vannucchi, G.4
Fallini, C.5
Persani, L.6
Beck-Peccoz, P.7
-
13
-
-
0037063119
-
Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism
-
Moreno JC, Bikker H, Kempers MJE, van Trotsenburg ASP, Baas F, de Vijlder JJM, Vulsma T & Ris-Stalpers C. Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism. New England Journal of Medicine 2002 347 95-102.
-
(2002)
New England Journal of Medicine
, vol.347
, pp. 95-102
-
-
Moreno, J.C.1
Bikker, H.2
Kempers, M.J.E.3
van Trotsenburg, A.S.P.4
Baas, F.5
de Vijlder, J.J.M.6
Vulsma, T.7
Ris-Stalpers, C.8
-
14
-
-
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. Human Biology 1992 64 531-538.
-
(1992)
Human Biology
, vol.64
, pp. 531-538
-
-
Lorey, F.W.1
Cunningham, G.C.2
-
17
-
-
0033924475
-
Risk factors for congenital hypothyroidism: An investigation of infant's birth weight, ethnicity, and gender in California 1990-1998
-
Waller DK, Anderson JL, Lorey F & Cunningham GC. Risk factors for congenital hypothyroidism: an investigation of infant's birth weight, ethnicity, and gender in California 1990-1998. Teratology 2000 62 36-41.
-
(2000)
Teratology
, vol.62
, pp. 36-41
-
-
Waller, D.K.1
Anderson, J.L.2
Lorey, F.3
Cunningham, G.C.4
-
18
-
-
0031933641
-
Congenital hypothyroidism in Wales (1982-1993): Demographic features, clinical presentation and effects on early neurodevelopment
-
Law WY, Bradley DM, Lazarus JH, John R & Gregory JW. Congenital hypothyroidism in Wales (1982-1993): demographic features, clinical presentation and effects on early neurodevelopment. Clinical Endocrinology 1998 48 201-207.
-
(1998)
Clinical Endocrinology
, vol.48
, pp. 201-207
-
-
Law, W.Y.1
Bradley, D.M.2
Lazarus, J.H.3
John, R.4
Gregory, J.W.5
-
19
-
-
0026500731
-
Congenital hypothyroidism detected by neonatal screening: Relationship between biochemical severity and early clinical features
-
Grant DB, Smith I, Fuggle PW, Tokar S & Chapple J. Congenital hypothyroidism detected by neonatal screening: relationship between biochemical severity and early clinical features. Archives of Diseases in Childhood 1992 67 87-90.
-
(1992)
Archives of Diseases in Childhood
, vol.67
, pp. 87-90
-
-
Grant, D.B.1
Smith, I.2
Fuggle, P.W.3
Tokar, S.4
Chapple, J.5
-
20
-
-
0033383706
-
Revised guidelines for neonatal screening programmes for primary congenital hypothyroidism
-
Working Group on Neonatal Screening of the European Society for Paediatric Endocrinology
-
Working Group on Neonatal Screening of the European Society for Paediatric Endocrinology, Revised guidelines for neonatal screening programmes for primary congenital hypothyroidism. Hormone Research 1999 52 49-52.
-
(1999)
Hormone Research
, vol.52
, pp. 49-52
-
-
-
21
-
-
0029084022
-
Weight at birth by gestational age in Italy
-
Parazzini F, Cortinovis I, Bortolus R, Fedele L & Decarli A. Weight at birth by gestational age in Italy. Human Reproduction 1995 10 1862-1863.
-
(1995)
Human Reproduction
, vol.10
, pp. 1862-1863
-
-
Parazzini, F.1
Cortinovis, I.2
Bortolus, R.3
Fedele, L.4
Decarli, A.5
-
22
-
-
18244368524
-
A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: Data from the Italian Registry for Congenital Hypothyroidism 1991-1998
-
Olivieri A, Stazi MA, Mastroiacovo P, Fazzini C, Medda E, Spagnolo A, De Angelis S, Grandolfo ME, Taruscio D, Cordeddu V & Sorcini M. A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism 1991-1998. Journal of Clinical Endocrinology and Metabolism 2002 87 557-562.
-
(2002)
Journal of Clinical Endocrinology and Metabolism
, vol.87
, pp. 557-562
-
-
Olivieri, A.1
Stazi, M.A.2
Mastroiacovo, P.3
Fazzini, C.4
Medda, E.5
Spagnolo, A.6
De Angelis, S.7
Grandolfo, M.E.8
Taruscio, D.9
Cordeddu, V.10
Sorcini, M.11
-
23
-
-
0002201951
-
Regional screening for congenital hypothyroidism: Results of screening one million North American infants with filter paper spot T4-TSH
-
Eds GN Burrow & JH Dussault. New York: Raven Press
-
Dussault JH, Mitchell ML, La Franchi S & Murphey WH. Regional screening for congenital hypothyroidism: results of screening one million North American infants with filter paper spot T4-TSH. In Neonatal Thyroid Screening, pp 155-165. Eds GN Burrow & JH Dussault. New York: Raven Press, 1980.
-
(1980)
Neonatal Thyroid Screening
, pp. 155-165
-
-
Dussault, J.H.1
Mitchell, M.L.2
La Franchi, S.3
Murphey, W.H.4
-
24
-
-
0028708550
-
Neonatal screening in congenital hypothyroidism in Italy
-
The National Registry
-
Sorcini M, Fazzini C, Olivieri A, Grandolfo ME, Medda E, Stazi MA, Balestrazzi P, Giovannelli G & Carta S. Neonatal screening in congenital hypothyroidism in Italy. The National Registry. Annali dell'Istituto Superiore di Sanità 1994 30 275-287.
-
(1994)
Annali Dell'Istituto Superiore Di Sanità
, vol.30
, pp. 275-287
-
-
Sorcini, M.1
Fazzini, C.2
Olivieri, A.3
Grandolfo, M.E.4
Medda, E.5
Stazi, M.A.6
Balestrazzi, P.7
Giovannelli, G.8
Carta, S.9
-
25
-
-
0015461988
-
Congenital hypothyroidism. Aetiological and clinical aspects
-
Maenpaa J. Congenital hypothyroidism. Aetiological and clinical aspects. Archives of Diseases in Childhood 1972 47 914-923.
-
(1972)
Archives of Diseases in Childhood
, vol.47
, pp. 914-923
-
-
Maenpaa, J.1
-
26
-
-
0032770581
-
Hypothyroxinemia in premature infants: Is thyroxine treatment necessary?
-
Fisher DA. Hypothyroxinemia in premature infants: is thyroxine treatment necessary? Thyroid 1999 9 715-720.
-
(1999)
Thyroid
, vol.9
, pp. 715-720
-
-
Fisher, D.A.1
-
28
-
-
0036284669
-
Gestational diabetes mellitus and neonatal hyperthyrotropinemia
-
Lao TT & Lee CP. Gestational diabetes mellitus and neonatal hyperthyrotropinemia. Gynecologic and Obstetric Investigation 2002 53 135-139.
-
(2002)
Gynecologic and Obstetric Investigation
, vol.53
, pp. 135-139
-
-
Lao, T.T.1
Lee, C.P.2
-
29
-
-
8044256495
-
Maternal nonthyroidal illness and fetal thyroid hormone status, as studied in the streptozotocin-induced diabetes mellitus rat model
-
Calvo R, Morreale De Escobar G, Escobar Del Rey F & Obregon MJ. Maternal nonthyroidal illness and fetal thyroid hormone status, as studied in the streptozotocin-induced diabetes mellitus rat model. Endocrinology 1997 138 1159-1169.
-
(1997)
Endocrinology
, vol.138
, pp. 1159-1169
-
-
Calvo, R.1
Morreale De Escobar, G.2
Escobar Del Rey, F.3
Obregon, M.J.4
-
30
-
-
0034500489
-
High frequency of antithyroid autoantibodies in pregnant women at increased risk of gestational diabetes mellitus
-
Olivieri A, Valensise H, Magnani F, Medda E, De Angelis S, D'archivio M, Sorcini M, Carta S & Romanini C. High frequency of antithyroid autoantibodies in pregnant women at increased risk of gestational diabetes mellitus. European Journal of Endocrinology 2000 143 741-747.
-
(2000)
European Journal of Endocrinology
, vol.143
, pp. 741-747
-
-
Olivieri, A.1
Valensise, H.2
Magnani, F.3
Medda, E.4
De Angelis, S.5
D'archivio, M.6
Sorcini, M.7
Carta, S.8
Romanini, C.9
-
31
-
-
29644446009
-
High risk of congenital hypothyroidism (CH) in twin pregnancies. Data from the Italian register for CH (1987-2000)
-
Abstracts of the 27th Annual Meeting of the European Thyroid Association. Warsaw, Poland, 25-29 August 2001
-
Olivieri A, Medda E, Fazzini C, Cotichini R, De Angelis S & Sorcini M. High risk of congenital hypothyroidism (CH) in twin pregnancies. Data from the Italian register for CH (1987-2000). Abstracts of the 27th Annual Meeting of the European Thyroid Association. Warsaw, Poland, 25-29 August 2001. Journal of Endocrinological Investigation 2001 24 (Suppl. to no. 6) 9.
-
(2001)
Journal of Endocrinological Investigation
, vol.24
, Issue.SUPPL. 6
, pp. 9
-
-
Olivieri, A.1
Medda, E.2
Fazzini, C.3
Cotichini, R.4
De Angelis, S.5
Sorcini, M.6
-
32
-
-
0031015706
-
Congenital anomalies in infants with congenital hypothyroidism: Is it a coincidental or an associated finding?
-
Al-Jurayyan NAM, Al-Herbish AS, El-Desouki MJ, Al-Nuaim AA, Abo-Bakr AM & Al-Husain MA. Congenital anomalies in infants with congenital hypothyroidism: is it a coincidental or an associated finding? Human Heredity 1997 47 33-37.
-
(1997)
Human Heredity
, vol.47
, pp. 33-37
-
-
Al-Jurayyan, N.A.M.1
Al-Herbish, A.S.2
El-Desouki, M.J.3
Al-Nuaim, A.A.4
Abo-Bakr, A.M.5
Al-Husain, M.A.6
-
33
-
-
0030991994
-
Population study of congenital hypothyroidism and associated birth defects, Atlanta 1979-1992
-
Roberts HE, Moore CA, Fernhoff PM, Brown AL & Khoury MJ. Population study of congenital hypothyroidism and associated birth defects, Atlanta 1979-1992. American Journal of Medical Genetics 1997 71 29-32.
-
(1997)
American Journal of Medical Genetics
, vol.71
, pp. 29-32
-
-
Roberts, H.E.1
Moore, C.A.2
Fernhoff, P.M.3
Brown, A.L.4
Khoury, M.J.5
-
34
-
-
0033548577
-
Congenital malformations in twins: An international study
-
Mastroiacovo P, Castilla EE, Arpino C, Botting B, Cocchi G, Goujard J, Marinacci C, Merlob P, Metneki J, Mutchinick O, Ritvanen A & Rosano A. Congenital malformations in twins: an international study. American Journal of Medical Genetics 1999 83 117-124.
-
(1999)
American Journal of Medical Genetics
, vol.83
, pp. 117-124
-
-
Mastroiacovo, P.1
Castilla, E.E.2
Arpino, C.3
Botting, B.4
Cocchi, G.5
Goujard, J.6
Marinacci, C.7
Merlob, P.8
Metneki, J.9
Mutchinick, O.10
Ritvanen, A.11
Rosano, A.12
-
37
-
-
0018832207
-
Lack of influence of thyroid antibodies on thyroid function in the newborn infant and on a mass screening program for congenital hypothyroidism
-
Dussault JH, Letarte J, Guyda H & Laberge C. Lack of influence of thyroid antibodies on thyroid function in the newborn infant and on a mass screening program for congenital hypothyroidism. Journal of Pediatrics 1980 96 385-389.
-
(1980)
Journal of Pediatrics
, vol.96
, pp. 385-389
-
-
Dussault, J.H.1
Letarte, J.2
Guyda, H.3
Laberge, C.4
-
38
-
-
0032622056
-
Thyroid function in mothers of hypothyroid newborns
-
Dussault JH & Fisher DA. Thyroid function in mothers of hypothyroid newborns. Obstetrics and Gynecology 1999 93 15-20.
-
(1999)
Obstetrics and Gynecology
, vol.93
, pp. 15-20
-
-
Dussault, J.H.1
Fisher, D.A.2
-
39
-
-
0141593619
-
Autoimmune thyroid disease and pregnancy: Relevance for the child
-
Dallas JS. Autoimmune thyroid disease and pregnancy: relevance for the child. Autoimmunity 2003 36 339-350.
-
(2003)
Autoimmunity
, vol.36
, pp. 339-350
-
-
Dallas, J.S.1
-
40
-
-
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. Journal of Clinical Endocrinology and Metabolism 1996 81 1147-1151.
-
(1996)
Journal of Clinical Endocrinology and Metabolism
, vol.81
, 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
-
41
-
-
0026968920
-
Comparison of epidemiological data on congenital hypothyroidism in Europe with those of the other parts in the world
-
Toublanc JE. Comparison of epidemiological data on congenital hypothyroidism in Europe with those of the other parts in the world. Hormone Research 1992 38 230-235.
-
(1992)
Hormone Research
, vol.38
, pp. 230-235
-
-
Toublanc, J.E.1
-
43
-
-
20844452197
-
Long term follow up of patients with inborn errors of metabolism detected by the newborn screening program in Japan
-
Aoki K. Long term follow up of patients with inborn errors of metabolism detected by the newborn screening program in Japan. Southeast Asian Journal of Tropical Medicine and Public Health 2003 3 (Suppl 3) 19-23.
-
(2003)
Southeast Asian Journal of Tropical Medicine and Public Health
, vol.3
, Issue.SUPPL. 3
, pp. 19-23
-
-
Aoki, K.1
-
45
-
-
0002642766
-
Status of iodine nutrition in Italy
-
Eds F Delange, JT Dunn & D Glinoer. New York: Plenum Press
-
Aghini-Lombardi F, Antonangeli L, Vitti P & Pinchera A. Status of iodine nutrition in Italy. In Iodine Deficiency in Europe: A Continuing Concern, vol. 241, pp 403-408. Eds F Delange, JT Dunn & D Glinoer. New York: Plenum Press, 1993.
-
(1993)
Iodine Deficiency in Europe: A Continuing Concern
, vol.241
, pp. 403-408
-
-
Aghini-Lombardi, F.1
Antonangeli, L.2
Vitti, P.3
Pinchera, A.4
-
48
-
-
0642367585
-
Iodine deficiency disorder incidence in neonates based on the experience with mass screening for congenital hypothyroidism in Southeast Poland in the years 1985-2000
-
Tylek-Lemanska D, Rybakowa M, Kumorowicz-Kopiec M, Dziatkowiak H & Ratajczak R. Iodine deficiency disorder incidence in neonates based on the experience with mass screening for congenital hypothyroidism in Southeast Poland in the years 1985-2000. Journal of Endocrinological Investigation 2003 26 32-38.
-
(2003)
Journal of Endocrinological Investigation
, vol.26
, pp. 32-38
-
-
Tylek-Lemanska, D.1
Rybakowa, M.2
Kumorowicz-Kopiec, M.3
Dziatkowiak, H.4
Ratajczak, R.5
-
49
-
-
0001236160
-
Iodine deficiency
-
Eds LE Braverman & RD Utiger. Philadelphia: Lippincott Williams and Wilkins
-
Delange F. Iodine deficiency. In The Thyroid: A Fundamental and Clinical Text, pp 295-316. Eds LE Braverman & RD Utiger. Philadelphia: Lippincott Williams and Wilkins, 2000.
-
(2000)
The Thyroid: A Fundamental and Clinical Text
, pp. 295-316
-
-
Delange, F.1
-
50
-
-
0032425156
-
Screening for congenital hypothyroidism used as an indicator of the degree of iodine deficiency and of its control
-
Delange F. Screening for congenital hypothyroidism used as an indicator of the degree of iodine deficiency and of its control. Thyroid 1998 8 1185-1192.
-
(1998)
Thyroid
, vol.8
, pp. 1185-1192
-
-
Delange, F.1
-
51
-
-
0024604830
-
Cytotoxic antibodies in congenital hypothyroidism
-
Bogner U, Gruters A, Sigle B, Helge H & Schleusener H. Cytotoxic antibodies in congenital hypothyroidism. Journal of Clinical Endocrinology and Metabolism 1989 68 671-675.
-
(1989)
Journal of Clinical Endocrinology and Metabolism
, vol.68
, pp. 671-675
-
-
Bogner, U.1
Gruters, A.2
Sigle, B.3
Helge, H.4
Schleusener, H.5
-
52
-
-
0026497302
-
Assessment of antibody dependent cell cytotoxicity in auto-immune thyroid disease using porcine thyroid cells
-
Rodien P, Madec AM, Morel Y, Stefanutti A, Bornet H & Orgiazzi J. Assessment of antibody dependent cell cytotoxicity in auto-immune thyroid disease using porcine thyroid cells. Autoimmunity 1992 13 177-185.
-
(1992)
Autoimmunity
, vol.13
, pp. 177-185
-
-
Rodien, P.1
Madec, A.M.2
Morel, Y.3
Stefanutti, A.4
Bornet, H.5
Orgiazzi, J.6
|