-
1
-
-
0013878213
-
Dwarfism and cortical thickening of tubular bones
-
Kenney FM, Linarelli L. Dwarfism and cortical thickening of tubular bones. Am J Dis Child 1966;111:201-7.
-
(1966)
Am J Dis Child
, vol.111
, pp. 201-207
-
-
Kenney, F.M.1
Linarelli, L.2
-
2
-
-
0014084874
-
Congenital stenosis of medullary spaces in tubular ones and calvaria in two proportional mother and son dwarfs, coupled with transitory hypocalcemic tetany
-
Caffey J. Congenital stenosis of medullary spaces in tubular ones and calvaria in two proportional mother and son dwarfs, coupled with transitory hypocalcemic tetany. Am J Roentgenol 1967;100:1-11.
-
(1967)
Am J Roentgenol
, vol.100
, pp. 1-11
-
-
Caffey, J.1
-
4
-
-
0032533602
-
The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43
-
Diaz GA, Khan KTS, Geib BD. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43. Genomics 1998;54:13-18.
-
(1998)
Genomics
, vol.54
, pp. 13-18
-
-
Diaz, G.A.1
Khan, K.T.S.2
Geib, B.D.3
-
5
-
-
0031055673
-
Kenny-Caffey syndrome in six bedouin sibships: Autosomal recessive inheritance is confirmed
-
Khan KTS, Uma R, Usha R, Al Ghanem MM, Al Awadi SA, Farag TI. Kenny-Caffey syndrome in six bedouin sibships: Autosomal recessive inheritance is confirmed. Am J Med Genet 1997;69:126-32.
-
(1997)
Am J Med Genet
, vol.69
, pp. 126-132
-
-
Khan, K.T.S.1
Uma, R.2
Usha, R.3
Al Ghanem, M.M.4
Al Awadi, S.A.5
Farag, T.I.6
-
6
-
-
0024560224
-
Kenny-Caffey syndrome: Case report and literature review
-
Abdel-Al YK, Auger LT, El-Gharbawy F. Kenny-Caffey syndrome: Case report and literature review. Clin Pediatr 1989;28:175-79.
-
(1989)
Clin Pediatr
, vol.28
, pp. 175-179
-
-
Abdel-Al, Y.K.1
Auger, L.T.2
El-Gharbawy, F.3
-
8
-
-
0032903371
-
Kenny-Caffey syndrome: An Arab variant?
-
Sabry MA, Farag TI, Shaltout AA, Zaki M, Al-Mazidi Z, Abulhassan SJ, Al-Torki N, Quishavi A, Al Awadi SA. Kenny-Caffey syndrome: An Arab variant? Clin Genet 1999;55:44-49.
-
(1999)
Clin Genet
, vol.55
, pp. 44-49
-
-
Sabry, M.A.1
Farag, T.I.2
Shaltout, A.A.3
Zaki, M.4
Al-Mazidi, Z.5
Abulhassan, S.J.6
Al-Torki, N.7
Quishavi, A.8
Al Awadi, S.A.9
-
9
-
-
0019435319
-
The Kenny syndrome: A rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism, and anomalies of refraction
-
Majewski F, Rosendahl W, Ranke M, Nolte K. The Kenny syndrome: A rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism, and anomalies of refraction. Eur J Pediatr 1981:136;21-30.
-
(1981)
Eur J Pediatr
, vol.136
, pp. 21-30
-
-
Majewski, F.1
Rosendahl, W.2
Ranke, M.3
Nolte, K.4
-
10
-
-
0026567026
-
Kenny-Caffey syndrome in two sibs born to consanguineous parents: Evidence for an autosomal recessive variant
-
Francheschini P, Testa A, Bogetti G, Girardo E, Gulala A, Lopez-Bell G, Buzio G, Ferrario E, Picatto E. Kenny-Caffey syndrome in two sibs born to consanguineous parents: Evidence for an autosomal recessive variant. Am J Med Genet 1992;42:112-16.
-
(1992)
Am J Med Genet
, vol.42
, pp. 112-116
-
-
Francheschini, P.1
Testa, A.2
Bogetti, G.3
Girardo, E.4
Gulala, A.5
Lopez-Bell, G.6
Buzio, G.7
Ferrario, E.8
Picatto, E.9
-
11
-
-
0022456215
-
Kenny syndrome: Evidence for idipathic hypoparathyroidism in two parents and for abnormal parathyroid hormone in bone
-
Fanconi S, Fischer JS, Wieland P, Atares M, Fanconi A, Giedion A, Prader A. Kenny syndrome: Evidence for idipathic hypoparathyroidism in two parents and for abnormal parathyroid hormone in bone. J Pediatr 1986;109:469-75.
-
(1986)
J Pediatr
, vol.109
, pp. 469-475
-
-
Fanconi, S.1
Fischer, J.S.2
Wieland, P.3
Atares, M.4
Fanconi, A.5
Giedion, A.6
Prader, A.7
-
12
-
-
0018340285
-
Ocular findings in Kenny's syndrome
-
Boynton JR, Pheasant TR, Jouhnson BL, Levin DB, Streeten BW. Ocular findings in Kenny's syndrome. Arch Opthtalmol 1979;97:896-900.
-
(1979)
Arch Opthtalmol
, vol.97
, pp. 896-900
-
-
Boynton, J.R.1
Pheasant, T.R.2
Jouhnson, B.L.3
Levin, D.B.4
Streeten, B.W.5
-
13
-
-
0023678492
-
Kenny syndrome: Description of additional abnormalities and molecular studies
-
Bergada I, Schiffrin A, Abu Srair H, Kaplan P, Dornan J, Goltzman D, Hendy GN. Kenny syndrome: Description of additional abnormalities and molecular studies. Hum Genet 1988;8039-42.
-
(1988)
Hum Genet
, pp. 8039-8042
-
-
Bergada, I.1
Schiffrin, A.2
Abu Srair, H.3
Kaplan, P.4
Dornan, J.5
Goltzman, D.6
Hendy, G.N.7
-
14
-
-
0020630549
-
Kenny-Caffey syndrome: Growth retardation and hypocalcemia in a young boy
-
Lee WK, Vargas A, Barnes J, Root AW. Kenny-Caffey syndrome: Growth retardation and hypocalcemia in a young boy. Am J Med Genet 1983;14:773-82.
-
(1983)
Am J Med Genet
, vol.14
, pp. 773-782
-
-
Lee, W.K.1
Vargas, A.2
Barnes, J.3
Root, A.W.4
-
15
-
-
0031792504
-
Kenney-Caffey syndrome and micro-orchidism
-
Hoffman WH, Kovacs K, Li S, Kulharya AS, Johnson BL, Eidson Ms, Cleveland WH. Kenney-Caffey syndrome and micro-orchidism. Am J Med Genet 1998;80:107-11.
-
(1998)
Am J Med Genet
, vol.80
, pp. 107-111
-
-
Hoffman, W.H.1
Kovacs, K.2
Li, S.3
Kulharya, A.S.4
Johnson, B.L.5
Eidson, M.6
Cleveland, W.H.7
-
16
-
-
0034304139
-
Craniofacial morphology, dental occlusion, tooth eruption, and dental maturity in boys of short stature with or without growth hormone deficiency
-
Kjellberg H, Beiring M, Wikland KA. Craniofacial morphology, dental occlusion, tooth eruption, and dental maturity in boys of short stature with or without growth hormone deficiency. Eur J Oral Sci 2000;108:359-67.
-
(2000)
Eur J Oral Sci
, vol.108
, pp. 359-367
-
-
Kjellberg, H.1
Beiring, M.2
Wikland, K.A.3
-
17
-
-
0017974591
-
Removable overdentures in the oral rehabilitation of patient with dentinogenesis imperfecta
-
Esposito S, Vergo TJ Jr. Removable overdentures in the oral rehabilitation of patient with dentinogenesis imperfecta. J Pedod 1978;2:304-15.
-
(1978)
J Pedod
, vol.2
, pp. 304-315
-
-
Esposito, S.1
Vergo Jr., T.J.2
-
19
-
-
0030154247
-
Dentinogenesis imperfecta: Influence of an overdenture on gingival tissues and tooth mobility
-
Cehreli ZC, Altay N. Dentinogenesis imperfecta: Influence of an overdenture on gingival tissues and tooth mobility. J Clin Pediatr Dent 1996;20:227-80.
-
(1996)
J Clin Pediatr Dent
, vol.20
, pp. 227-280
-
-
Cehreli, Z.C.1
Altay, N.2
-
20
-
-
0018157802
-
Alveolar bone loss in overdentures: A five-year study
-
Crum RJ, Rooney GE Jr. Alveolar bone loss in overdentures: A five-year study. J Prosthet Dent 1978;40:610-13.
-
(1978)
J Prosthet Dent
, vol.40
, pp. 610-613
-
-
Crum, R.J.1
Rooney Jr., G.E.2
-
21
-
-
0017970691
-
Clinical comparison of masticatory performance and electromyographic activity of patients with complete dentures, overdentures, and natural teeth
-
Rissin L, House JE, Manly RS, Kapur KK. Clinical comparison of masticatory performance and electromyographic activity of patients with complete dentures, overdentures, and natural teeth. J Prosthet Dent 1978;39:508-11.
-
(1978)
J Prosthet Dent
, vol.39
, pp. 508-511
-
-
Rissin, L.1
House, J.E.2
Manly, R.S.3
Kapur, K.K.4
-
22
-
-
0035487927
-
Prosthodontics for pediatric patients with congenital/developmental orofacial anomalies: A long-term follow-up
-
Vergo TJ Jr. Prosthodontics for pediatric patients with congenital/developmental orofacial anomalies: A long-term follow-up. J Prosthet Dent 2001;86:342-47.
-
(2001)
J Prosthet Dent
, vol.86
, pp. 342-347
-
-
Vergo Jr., T.J.1
-
23
-
-
0024074799
-
Complete overlay dentures for the pediatric patient: Case reports
-
Schneidman E, Wilson S, Spuller RL. Complete overlay dentures for the pediatric patient: Case reports. Pediatr Dent 1988;10:222-25.
-
(1988)
Pediatr Dent
, vol.10
, pp. 222-225
-
-
Schneidman, E.1
Wilson, S.2
Spuller, R.L.3
-
24
-
-
0037929123
-
The use of overdentures in the management of severe hypodontia associated with microdontia: A case report
-
Cengiz SB, Stephen A. The use of overdentures in the management of severe hypodontia associated with microdontia: A case report. J Clin Pediatr Dent 2003;27:219-22.
-
(2003)
J Clin Pediatr Dent
, vol.27
, pp. 219-222
-
-
Cengiz, S.B.1
Stephen, A.2
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