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SINDROME DE PENDRED. COMUNICACION DE DOS CASOS FAMILIARES. = SYNDROME DE PENDRED. COMMUNICATION DE 2 CAS FAMILIAUXNUNO DE LA ROSA POZUELO JA; CLAVER VALDERAS MA; SANZ GARCIA D et al.1977; REV. CLIN. ESP.; ESP.; DA. 1977; VOL. 147; NO 5; PP. 523-526; BIBL. 7 REF.Article

DISSOCIATED THYROXINE, TRIIODOTHYRONINE AND REVERSE TRIIODOTHYRONINE LEVELS IN PATIENTS WITH FAMILIAL GOITRE DUE TO IODIDE ORGANIFICATION DEFECTSCHAN V; WANG C; YEUNG RTT et al.1979; CLIN. ENDOCRINOL.; GBR; DA. 1979; VOL. 11; NO 3; PP. 257-265; BIBL. 23 REF.Article

ZUR ABKLAERUNG GENETISCH BEDINGTER SCHWERHOERIGKEIT: 5 FAELLE VON PENDRED-SYNDROM = L'EXPLICATION DE LA SURDITE D'ORIGINE GENETIQUE: 5 CAS DE SYNDROME DE PENDREDHOERMANN K; HELD KR.1980; H.N.O.; DEU; DA. 1980; VOL. 28; NO 6; PP. 206-208; ABS. ENG; BIBL. 13 REF.Article

BIOCHEMICAL STUDIES ON THE IODINE ORGANIFICATION DEFECT OF PENDRED'S SYNDROMENIEPOMNISZCZE H; COLEONI AH; DEGROSSI OJ et al.1978; ACTA ENDOCRINOL.; DNK; DA. 1978; VOL. 89; NO 1; PP. 70-79; BIBL. 28 REF.Article

STUDIO ECOCARDIOGRAFICO IN DUE CASI DI SINDROME DI PENDRED = ETUDE ECHOCARDIOGRAPHIQUE DANS 2 CAS DE SYNDROME DE PENDREDPAGGI A; CASSONE R; LUCISANO V et al.1982; MINERVA MED.; ISSN 0026-4806; ITA; DA. 1982; VOL. 73; NO 14; PP. 796; ABS. ENG; BIBL. 16 REF.Article

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UN CAS DE SYNDROME DE PENDRED: ETUDE DE L'ANOMALIE FONCTIONNELLE AU NIVEAU MOLECULAIREABDELMOUMENE NAFISSA.sd; FRA; DA. S.D.; 50 P.-PL.; 30 CM; BIBL. 115 REF.; TH.: MED./ALGER/1978Thesis

THYROIDAL IODOPROTEINS IN PENDRED'S SYNDROME = IODOPROTEINES THYROIDIENNES DANS LE SYNDROME DE PENDREDDESAI KB; MEHTA MN; PATEL MC et al.1974; J. ENDOCRINOL.; G.B.; DA. 1974; VOL. 63; NO 2; PP. 409-410; H.T. 1; BIBL. 9REF.Article

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THE CONCENTRATION OF PEROXIDASE IN NORMAL AND ADENOMATOUS HUMAN THYROID TISSUE WITH SPECIAL REFERENCE TO PATIENTS WITH PENDRED'S SYNDROME = CONCENTRATION DE PEROXYDASE DANS LE TISSU THYROIDIEN HUMAIN NORMAL ET ADENOMATEUX AVEC MENTION SPECIALE CHEZ DES MALADES AVEC UN SYNDROME DE PENDREDLJUNGGREN JG; LINDSTROEM H; HJERN B et al.1973; ACTA ENDOCRINOL.; DANEM.; DA. 1973; VOL. 72; NO 2; PP. 272-278; BIBL. 21REF.Article

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ETUDE DE L'HORMONEMIE THYROIDIENNE DANS UNE POPULATION DE 98 ENFANTS HANDICAPES AUDITIFSCOLL J; DUTAU G; HOFF et al.1978; J. FR. OTO-RHINO-LARYNGOL.; FRA; DA. 1978; VOL. 27; NO 10; PP. 705-708; (3 P.)Article

THYROID CARCINOMA IN PENDRED'S SYNDROME.ILLUM P.1978; J. LARYNGOL. OTOL.; G.B.; DA. 1978; VOL. 92; NO 5; PP. 435-439; BIBL. 13 REF.Article

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THE CHANGES OF SERUM TRIIODOTHYRONINE, THYROXINE AND THYROID STIMULATING HORMONE IN TWO CASES OF HYPOTHYROIDISM WITH UNUSUAL COMPLICATIONS = MODIFICATIONS DE LA TRIIODOTHYRONINE, DE LA THYROXINE ET DE L'HORMONE THYREOTROPE SERIQUES DANS DEUX CAS D'HYPOTHYROIDIE AVEC DES COMPLICATIONS INHABITUELLESSAKURADA T; SAITO S; YAMAGUCHI T et al.1974; TOHOKU J. EXPER. MED.; JAP.; DA. 1974; VOL. 112; NO 4; PP. 365-371; BIBL. 9REF.Article

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Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutationsPRASAD, Sai; KÖLLN, Karen A; CUCCI, Robert A et al.American journal of medical genetics. 2004, Vol 124A, Num 1, pp 1-9, issn 0148-7299, 9 p.Article

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