Hereditary continuous muscle fiber activityMCGUIRE, S. A; TOMASOVIC, J. J; ACKERMAN, N. JR et al.Archives of neurology (Chicago). 1984, Vol 41, Num 4, pp 395-396, issn 0003-9942Article

Familial acromegalyJONES, M. K; EVANS, P. J; JONES, I. R et al.Clinical endocrinology (Oxford. Print). 1984, Vol 20, Num 3, pp 355-358, issn 0300-0664Article

Alcohol consumption of patients with essential tremorRAUTAKORPI, I; MARTTILA, R. J; RINNE, U. K et al.Acta neurologica scandinavica. 1983, Vol 68, Num 3, pp 177-179, issn 0001-6314Article

Essential familial myoclonusPRZUNTEK, H; MUHR, H.Journal of neurology. 1983, Vol 230, Num 3, pp 153-162, issn 0340-5354Article

Zur Frage der Erblichkeit der Vitiligo = Le problème de l'hérédité du vitiligo = The question of heredity in vitiligoSALAMON, T; HADZISELIMOVIC, R; HALEPOVIC, E et al.Hautarzt. 1989, Vol 40, Num 3, pp 141-145, issn 0017-8470Article

Hereditary angio-edema (HAE)BLOK, P. H. H. M; BAARSMA, E. A.Journal of laryngology and otology. 1984, Vol 98, Num 1, pp 59-63, issn 0022-2151Article

Muscle weakness in an adult with infantile X-linked hypogammaglobulinemiaMONTANARO, A; BARDANA, E. J. JR.Annals of allergy. 1984, Vol 52, Num 3, pp 153-154, issn 0003-4738Article

Alcoholism in essential tremorKOLLER, W. C.Neurology. 1983, Vol 33, Num 8, pp 1074-1076, issn 0028-3878Article

Histochemical study of rectal aminergic nerves in type I familial amyloid polyneuropathyIKEDA, S; OGUCHI, K; KOBAYASHI, S et al.Neurology. 1983, Vol 33, Num 8, pp 1055-1058, issn 0028-3878Article

Biochemical studies on the purine metabolism of four cases with hereditary xanthinuriaKOJIMA, T; NISHINA, T; KITAMURA, M et al.Clinica chimica acta. 1984, Vol 137, Num 2, pp 189-198, issn 0009-8981Article

Familial colonic cancer without antecedent polyposisBOLAND, C. R; TRONCALE, F. J.Annals of internal medicine. 1984, Vol 100, Num 5, pp 700-701, issn 0003-4819Article

Chorée familiale, non progressive, liée au sexe = Hereditary, X linked non progressive choreaLANDRIEU, P; BENCHET, M. L; TARDIEU, M et al.Revue neurologique (Paris). 1984, Vol 140, Num 6-7, pp 432-433, issn 0035-3787Article

Acrodermatitis enteropathica, erbliche Parakeratose der Kälber: Beitrag zur Vergleichen Dermatologie = Acrodermatitis enteropathica: parakératose héréditaire des veaux. Contribution à la dermatologie comparative = Acrodermatitis enteropathica: hereditary parakeratosis of calves. Contribution to comparative dermatologyREICH, H.H + G. Zeitschrift für Hautkrankheiten. 1983, Vol 58, Num 19, pp 1410-1415, issn 0301-0481Article

Esquisse d'une histoire de la dystrophie thrombocytaire hémorragipare congénitale = Brief case history of congenital hemorrhagic thrombocytic dystrophyBERNARD, J; BELLUCHI, S.Actualités hématologiques. 1983, Vol 17, pp 3-13, issn 0567-8757Article

Hereditary hormone excess : Genes, molecular pathways, and syndromesMARX, Stephen J; SIMONDS, William F.Endocrine reviews. 2005, Vol 26, Num 5, pp 615-661, issn 0163-769X, 47 p.Article

Gastroduodenal polyps in familial polyposis coliGAHTAN, V; NOCHOMOVITZ, L. E; ROBINSON, A. M et al.The American surgeon. 1989, Vol 55, Num 5, pp 278-280, issn 0003-1348, 3 p.Article

Bromocriptine and genetic hypertension development in young spontaneously hypertensive ratsRICHER, C; LHOSTE, F; GIUDICELLI, J.-F et al.Journal de pharmacologie. 1984, Vol 15, Num 2, pp 185-197, issn 0021-793XArticle

Pharmacological characterization of apomorphine-induced hypothermia in the spontaneously hypertensive ratMARTIN, J. R; QUOCK, R. M.Life sciences (1973). 1984, Vol 35, Num 9, pp 929-936, issn 0024-3205Article

Hereditary α₂-antiplasmin deficiencySTORMORKEN, H; GOGSTAD, G. O; BROSSTAD, F et al.Thrombosis research. 1983, Vol 31, Num 4, pp 647-651, issn 0049-3848Article

A role for MLH3 in hereditary nonpolyposis colorectal cancerYING WU; BERENDS, Maran J. W; BUYS, Charles H. C. M et al.Nature genetics. 2001, Vol 29, Num 2, pp 137-138, issn 1061-4036Article

Akrokeratoderma hereditarium punctatum = Acrokératodermie ponctuée héréditaire = Acrokeratoderma hereditarium punctatumWERNI, R; SCHWARZ, T; GSCHNAIT, F et al.H + G. Zeitschrift für Hautkrankheiten. 1984, Vol 59, Num 1, pp 37-40, issn 0301-0481Article

Benign familial chorea: an association with intellectual impairmentLELI, D. A; FURLOW, T. W. JR; FALGOUT, J. C et al.Journal of neurology, neurosurgery and psychiatry. 1984, Vol 47, Num 5, pp 471-474, issn 0022-3050Article

Cancer familial du côlon sans polypose et syndrome familial du cancer = Familial carcinoma of the colon without polyposis and cancer family syndromePOISSONNIER, M; ANDRIEU, J; GARDON, J.-D et al.Journal de génétique humaine. 1983, Vol 31, Num 4, pp 255-278, issn 0021-7743Article

TOM : enhancement and extension of a tool suite for in silico approaches to multigenic hereditary disordersMASOTTI, Daniele; NARDINI, Christine; ROSSI, Simona et al.Bioinformatics (Oxford. Print). 2008, Vol 24, Num 3, pp 428-429, issn 1367-4803, 2 p.Article

Hereditary dysfibrinogenemia in a patient with thrombotic diseaseCARREL, N; GABRIEL, D. A; BLATT, P. M et al.Blood. 1983, Vol 62, Num 2, pp 439-447, issn 0006-4971Article