-
1
-
-
70449232246
-
Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness
-
CH Alström B Hallgren LB Nilsson H Åsander Retinal degeneration combined with obesity, diabetes mellitus and neurogenous deafness Acta Psychiatr Neurol Scand 34 suppl 129 1959 1 35
-
(1959)
Acta Psychiatr Neurol Scand
, vol.34
, Issue.suppl 129
, pp. 1-35
-
-
Alström, CH1
Hallgren, B2
Nilsson, LB3
Åsander, H4
-
2
-
-
0014696328
-
Familial syndrome of primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities
-
RL Weinstein B Kliman RE Scully Familial syndrome of primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities N Engl J Med 281 1969 969 977
-
(1969)
N Engl J Med
, vol.281
, pp. 969-977
-
-
Weinstein, RL1
Kliman, B2
Scully, RE3
-
3
-
-
0014605392
-
The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland: clinical, genetic and epidemiological studies
-
D Klein F Ammann The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland: clinical, genetic and epidemiological studies J Neurol Sci 9 1969 479 513
-
(1969)
J Neurol Sci
, vol.9
, pp. 479-513
-
-
Klein, D1
Ammann, F2
-
4
-
-
0015535502
-
The Alström syndrome: report of three cases with further delineation of the clinical, pathophysiological and genetic aspects of the disorder
-
JL Goldstein PJ Fialkow The Alström syndrome: report of three cases with further delineation of the clinical, pathophysiological and genetic aspects of the disorder Medicine 52 1973 53 71
-
(1973)
Medicine
, vol.52
, pp. 53-71
-
-
Goldstein, JL1
Fialkow, PJ2
-
5
-
-
0021647930
-
The Alström syndrome: ophthalmic histopathology and retinal ultrastructure
-
J Sebag DM Albert JL Craft The Alström syndrome: ophthalmic histopathology and retinal ultrastructure Br J Ophthalmol 68 1984 494 501
-
(1984)
Br J Ophthalmol
, vol.68
, pp. 494-501
-
-
Sebag, J1
Albert, DM2
Craft, JL3
-
6
-
-
0022973179
-
Ophthalmologic and systemic manifestations of Alström's disease
-
RH Millay RG Weleber JR Heckenlively Ophthalmologic and systemic manifestations of Alström's disease Am J Ophthalmol 102 1986 482 490
-
(1986)
Am J Ophthalmol
, vol.102
, pp. 482-490
-
-
Millay, RH1
Weleber, RG2
Heckenlively, JR3
-
7
-
-
0023484651
-
Late-onset dilated cardiomyopathy in a unique familial syndrome of hypogonadism and metabolic abnormalities
-
SE Warren SJ Schnitt AJ Bauman Late-onset dilated cardiomyopathy in a unique familial syndrome of hypogonadism and metabolic abnormalities Am Heart J 114 1987 1522 1524
-
(1987)
Am Heart J
, vol.114
, pp. 1522-1524
-
-
Warren, SE1
Schnitt, SJ2
Bauman, AJ3
-
8
-
-
0025003980
-
Alström's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction
-
SJ Charles AT Moore JRW Yates T Green P Clark Alström's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction J Med Genet 27 1990 590 592
-
(1990)
J Med Genet
, vol.27
, pp. 590-592
-
-
Charles, SJ1
Moore, AT2
Yates, JRW3
Green, T4
Clark, P5
-
10
-
-
0027469341
-
Growth hormone deficiency in two siblings with Alström syndrome
-
CA Alter T Moshang Growth hormone deficiency in two siblings with Alström syndrome Am J Dis Child 147 1993 97 99
-
(1993)
Am J Dis Child
, vol.147
, pp. 97-99
-
-
Alter, CA1
Moshang, T2
-
11
-
-
0027232213
-
Longitudinal study of the early electroretinographic changes in Alström's syndrome
-
F Tremblay RG LaRoche SE Shea MD Ludman Longitudinal study of the early electroretinographic changes in Alström's syndrome Am J Ophthalmol 115 1993 657 665
-
(1993)
Am J Ophthalmol
, vol.115
, pp. 657-665
-
-
Tremblay, F1
LaRoche, RG2
Shea, SE3
Ludman, MD4
-
14
-
-
0018774245
-
Exploration électrophysiologique fonctionnelle, sectorielle et stratigraphique de la fonction visuelle
-
R Alfieri P Sole Exploration électrophysiologique fonctionnelle, sectorielle et stratigraphique de la fonction visuelle J Fr Biophys Med Nucl 2 1979 63 75
-
(1979)
J Fr Biophys Med Nucl
, vol.2
, pp. 63-75
-
-
Alfieri, R1
Sole, P2
-
16
-
-
0024729184
-
Les problèmes électrorétinographiques du diagnostic des affections des cônes et de la macula
-
JC Hache S Defoort B Puech F Bale E Mancel Les problèmes électrorétinographiques du diagnostic des affections des cônes et de la macula Ophtalmologie 3 1989 279 282
-
(1989)
Ophtalmologie
, vol.3
, pp. 279-282
-
-
Hache, JC1
Defoort, S2
Puech, B3
Bale, F4
Mancel, E5
-
17
-
-
0027172743
-
Dystrophin expression in the human retina is required for normal function as defined by electroretinography
-
DM Pillers DE Bulman RG Weleber Dystrophin expression in the human retina is required for normal function as defined by electroretinography Nature Genetics 4 1993 82 86
-
(1993)
Nature Genetics
, vol.4
, pp. 82-86
-
-
Pillers, DM1
Bulman, DE2
Weleber, RG3
-
19
-
-
0018602014
-
Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance
-
National Diabetes Data Group Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance Diabetes 28 1979 1039 1057
-
(1979)
Diabetes
, vol.28
, pp. 1039-1057
-
-
National Diabetes Data Group1
-
20
-
-
0017091564
-
The clinical course of primary myocardial disease in infants and children
-
RD Greenwood AS Nadas DC Fyler The clinical course of primary myocardial disease in infants and children Am Heart J 92 1976 549 560
-
(1976)
Am Heart J
, vol.92
, pp. 549-560
-
-
Greenwood, RD1
Nadas, AS2
Fyler, DC3
-
21
-
-
0021959005
-
Findings on endomyocardial biopsy in infants and children with dilated cardiomyopathy
-
AB Lewis HB Neustein M Takahashi PR Lurie Findings on endomyocardial biopsy in infants and children with dilated cardiomyopathy Am J Cardiol 55 1985 143 145
-
(1985)
Am J Cardiol
, vol.55
, pp. 143-145
-
-
Lewis, AB1
Neustein, HB2
Takahashi, M3
Lurie, PR4
-
22
-
-
0023821096
-
Natural history and prognostic factors in endocardial fibroelastosis
-
T Ino LN Benson RM Freedom RD Rowe Natural history and prognostic factors in endocardial fibroelastosis Am J Cardiol 62 1988 431 434
-
(1988)
Am J Cardiol
, vol.62
, pp. 431-434
-
-
Ino, T1
Benson, LN2
Freedom, RM3
Rowe, RD4
-
24
-
-
0025916726
-
Outcome of infants and children with dilated cardiomyopathy
-
AB Lewis M Chabot Outcome of infants and children with dilated cardiomyopathy Am J Cardiol 68 1991 365 369
-
(1991)
Am J Cardiol
, vol.68
, pp. 365-369
-
-
Lewis, AB1
Chabot, M2
-
25
-
-
0026319459
-
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
-
VV Michels P Moll FA Miller The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy N Engl J Med 326 1992 7782
-
(1992)
N Engl J Med
, vol.326
, pp. 7782
-
-
Michels, VV1
Moll, P2
Miller, FA3
-
26
-
-
0017282796
-
A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance
-
JA Edwards PK Sethi AJ Scoma RM Bannerman LA Frohman A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance Am J Med 60 1976 23 32
-
(1976)
Am J Med
, vol.60
, pp. 23-32
-
-
Edwards, JA1
Sethi, PK2
Scoma, AJ3
Bannerman, RM4
Frohman, LA5
-
27
-
-
0027411211
-
Familial insulin-resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deafness and mental retardation
-
R Boor J Herwig J Schrezenmeir BF Pontz W Schönberger Familial insulin-resistant diabetes associated with acanthosis nigricans, polycystic ovaries, hypogonadism, pigmentary retinopathy, labyrinthine deafness and mental retardation Am J Med Genet 45 1993 649 653
-
(1993)
Am J Med Genet
, vol.45
, pp. 649-653
-
-
Boor, R1
Herwig, J2
Schrezenmeir, J3
Pontz, BF4
Schönberger, W5
-
28
-
-
0024472754
-
The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome
-
JS Green PS Parfrey JD Harnett The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome N Engl J Med 321 1989 1002 1009
-
(1989)
N Engl J Med
, vol.321
, pp. 1002-1009
-
-
Green, JS1
Parfrey, PS2
Harnett, JD3
-
29
-
-
2442769311
-
Heart disease in the Laurence-Moon-Biedl-Bardet syndrome
-
TG McLoughlin LJ Krovetz GL Schiebler Heart disease in the Laurence-Moon-Biedl-Bardet syndrome J Pediatr 65 1964 388 399
-
(1964)
J Pediatr
, vol.65
, pp. 388-399
-
-
McLoughlin, TG1
Krovetz, LJ2
Schiebler, GL3
-
30
-
-
0027963165
-
Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patients
-
K Elbedour N Zucker E Zalzstein Y Barki R Carmi Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patients Am J Med Genet 52 1994 164 169
-
(1994)
Am J Med Genet
, vol.52
, pp. 164-169
-
-
Elbedour, K1
Zucker, N2
Zalzstein, E3
Barki, Y4
Carmi, R5
-
31
-
-
0025367613
-
Patterns of rod and cone dysfunction in Bardet-Biedl syndrome
-
SG Jacobson F-X Borruat PP Apáthy Patterns of rod and cone dysfunction in Bardet-Biedl syndrome Am J Ophthalmol 109 1990 676 688
-
(1990)
Am J Ophthalmol
, vol.109
, pp. 676-688
-
-
Jacobson, SG1
Borruat, F-X2
Apáthy, PP3
-
32
-
-
0027383341
-
Natural course of visual functions in the Bardet-Biedl syndrome
-
Ab Fulton RM Hansen RJ Glynn Natural course of visual functions in the Bardet-Biedl syndrome Arch Ophthalmol 111 1993 1500 1506
-
(1993)
Arch Ophthalmol
, vol.111
, pp. 1500-1506
-
-
Fulton, Ab1
Hansen, RM2
Glynn, RJ3
-
33
-
-
0020057211
-
Bardet-Biedl syndrome and related disorders
-
AP Schachat IH Maumenee Bardet-Biedl syndrome and related disorders Arch Ophthalmol 100 1982 285 288
-
(1982)
Arch Ophthalmol
, vol.100
, pp. 285-288
-
-
Schachat, AP1
Maumenee, IH2
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