-
1
-
-
15844377656
-
Congenital cutaneous dystrophy (Thomson's type)
-
Rook A, Whimster I: Congenital cutaneous dystrophy (Thomson's type). Br J Dermatol 61:197-205, 1949.
-
(1949)
Br J Dermatol
, vol.61
, pp. 197-205
-
-
Rook, A.1
Whimster, I.2
-
2
-
-
0024078016
-
Le syndrome de Rothmund-Thomson: À propos de quatre cas
-
Paris
-
Sfar Z, Rihane E, Kamoun MR: Le syndrome de Rothmund-Thomson: à propos de quatre cas. Ann Pédiatr (Paris) 35:501-506, 1988.
-
(1988)
Ann Pédiatr
, vol.35
, pp. 501-506
-
-
Sfar, Z.1
Rihane, E.2
Kamoun, M.R.3
-
3
-
-
0013882044
-
Rothmund-Thomson syndrome: An oculocutaneus disorder
-
Silver HK: Rothmund-Thomson syndrome: An oculocutaneus disorder. Am J Dis Child 111:182-190, 1966.
-
(1966)
Am J Dis Child
, vol.111
, pp. 182-190
-
-
Silver, H.K.1
-
4
-
-
0017038639
-
Le syndrome de Rothmund: À propos d'une observation
-
Ourgaud A, Payan H, Giraud F: Le syndrome de Rothmund: à propos d'une observation. J Genet Hum 24 (Suppl): 151-164, 1976.
-
(1976)
J Genet Hum
, vol.24
, Issue.SUPPL.
, pp. 151-164
-
-
Ourgaud, A.1
Payan, H.2
Giraud, F.3
-
5
-
-
0020576231
-
Syndrome de Rothmund-Thomson avec glaucome: Étude endocrinienne
-
Nathanson M, Dandine M, Gaudelus J: Syndrome de Rothmund-Thomson avec glaucome: étude endocrinienne. Ann Pediatr 30: 520-525, 1983.
-
(1983)
Ann Pediatr
, vol.30
, pp. 520-525
-
-
Nathanson, M.1
Dandine, M.2
Gaudelus, J.3
-
6
-
-
0020395084
-
Un cas de maladie de Rothmund-Thomson avec hypertension
-
Dechenne C, Brumioul D, Chantraine JM: Un cas de maladie de Rothmund-Thomson avec hypertension. Ann Pediatr 29:665, 1982.
-
(1982)
Ann Pediatr
, vol.29
, pp. 665
-
-
Dechenne, C.1
Brumioul, D.2
Chantraine, J.M.3
-
7
-
-
0018874031
-
Epilepsy and myopathy in a patient with Rothmund-Thomson's syndrome
-
Lessem J, Bierre I, Forslund M: Epilepsy and myopathy in a patient with Rothmund-Thomson's syndrome. Acta Med Scand 207:237-239, 1980.
-
(1980)
Acta Med Scand
, vol.207
, pp. 237-239
-
-
Lessem, J.1
Bierre, I.2
Forslund, M.3
-
8
-
-
0018502429
-
Rothmund-Thomson syndrome (poikiloderma congenital) in two sisters
-
Srivastava RN, Azami S, Bhan MK: Rothmund-Thomson syndrome (poikiloderma congenital) in two sisters. Indian Pediatr 16:715-718, 1979.
-
(1979)
Indian Pediatr
, vol.16
, pp. 715-718
-
-
Srivastava, R.N.1
Azami, S.2
Bhan, M.K.3
-
9
-
-
0023269451
-
Rothmund-Thomson syndrome: A case report, phototesting, and literature review
-
Berg E, Chuang TY, Cripps D: Rothmund-Thomson syndrome: A case report, phototesting, and literature review. J Am Acad Dermatol 17:332-338, 1987.
-
(1987)
J Am Acad Dermatol
, vol.17
, pp. 332-338
-
-
Berg, E.1
Chuang, T.Y.2
Cripps, D.3
-
10
-
-
0023433796
-
Poïkilodermie de Rothmund-Thomson: À propos du suivi sur vingt ans d'un cas déjà présenté dans la petite enfance
-
Paris
-
Plantin P, Castel Y, Masse R: Poïkilodermie de Rothmund-Thomson: À propos du suivi sur vingt ans d'un cas déjà présenté dans la petite enfance. Ann Pédiatr (Paris) 34:635-638, 1987.
-
(1987)
Ann Pédiatr
, vol.34
, pp. 635-638
-
-
Plantin, P.1
Castel, Y.2
Masse, R.3
-
11
-
-
3242804840
-
Rothmund's syndrome-Thomson's syndrome
-
Taylor WB. Rothmund's syndrome-Thomson's syndrome. Arch Dermatol 75:236-244, 1957.
-
(1957)
Arch Dermatol
, vol.75
, pp. 236-244
-
-
Taylor, W.B.1
-
12
-
-
0020986434
-
Poïkilodermie congénitale (syndrome de Rothmund-Thomson)
-
Vallet C, Prigent G, Jeanmougin M: Poïkilodermie congénitale (syndrome de Rothmund-Thomson). Ann Dermatol Venereol 110: 773-774, 1983.
-
(1983)
Ann Dermatol Venereol
, vol.110
, pp. 773-774
-
-
Vallet, C.1
Prigent, G.2
Jeanmougin, M.3
-
13
-
-
0017667929
-
Das Thomson-syndrom: Ein Beitrag zu den kongenitalen Poikilodermien
-
Rodermund OE, Hausmann D; Das Thomson-syndrom: Ein Beitrag zu den kongenitalen Poikilodermien. Dermatol Monatsschr 163:601-612, 1977.
-
(1977)
Dermatol Monatsschr
, vol.163
, pp. 601-612
-
-
Rodermund, O.E.1
Hausmann, D.2
-
14
-
-
0017724509
-
Une observation de poïkilodermie congénitale (syndrome de Rothmund-Thomson) avec dystrophies majeures, nanisme très sévère et intolérance digestive
-
Castel Y, Masse R, Toudic L: Une observation de poïkilodermie congénitale (syndrome de Rothmund-Thomson) avec dystrophies majeures, nanisme très sévère et intolérance digestive. Ann Pediatr 24:647-651, 1977.
-
(1977)
Ann Pediatr
, vol.24
, pp. 647-651
-
-
Castel, Y.1
Masse, R.2
Toudic, L.3
-
15
-
-
0023259214
-
Epidermal dysplasia and skeletal deformity in congenital poikiloderma (Rothmund-Thomson syndrome)
-
Shuttleworth D, Marks R: Epidermal dysplasia and skeletal deformity in congenital poikiloderma (Rothmund-Thomson syndrome). Br J Dermatol 117:377-384, 1987.
-
(1987)
Br J Dermatol
, vol.117
, pp. 377-384
-
-
Shuttleworth, D.1
Marks, R.2
-
16
-
-
0024802636
-
The poikiloderma of Rothmund-Thomson syndrome: Changes in Langherans cell morphology and distribution
-
Sillevis-Smitt JH, Gons MH, Oorthuys JW: The poikiloderma of Rothmund-Thomson syndrome: Changes in Langherans cell morphology and distribution. Dermatologica 179:187-190, 1989.
-
(1989)
Dermatologica
, vol.179
, pp. 187-190
-
-
Sillevis-Smitt, J.H.1
Gons, M.H.2
Oorthuys, J.W.3
-
17
-
-
0025727468
-
Poikiloderma congenital: Case report and review of the literature
-
Collins P, Barnes L, McCabe M: Poikiloderma congenital: Case report and review of the literature. Pediatr Dermatol 8:58-60, 1991
-
(1991)
Pediatr Dermatol
, vol.8
, pp. 58-60
-
-
Collins, P.1
Barnes, L.2
McCabe, M.3
-
18
-
-
84993924495
-
The Rothmund-Thomson syndrome: Case report of an unusual syndrome
-
Oates RK, Lewis MB, Walker-Smith JA: The Rothmund-Thomson syndrome: Case report of an unusual syndrome. Aust Paediatr J 7:103-107, 1991.
-
(1991)
Aust Paediatr J
, vol.7
, pp. 103-107
-
-
Oates, R.K.1
Lewis, M.B.2
Walker-Smith, J.A.3
-
22
-
-
0018842911
-
Rothmund-Thomson syndrome wih severe dwarfism
-
Hall JG, Pagon RA, Wilson KM: Rothmund-Thomson syndrome wih severe dwarfism. Am J Dis Child 143:165-169, 1980.
-
(1980)
Am J Dis Child
, vol.143
, pp. 165-169
-
-
Hall, J.G.1
Pagon, R.A.2
Wilson, K.M.3
-
23
-
-
0016834543
-
Hypogonadism and parathyroid adenoma in congenital poikiloderma (Rothmund-Thomson syndrome)
-
Werder EA, Murset G, Illig R: Hypogonadism and parathyroid adenoma in congenital poikiloderma (Rothmund-Thomson syndrome). Clin Endocrinol 4:75-82, 1975.
-
(1975)
Clin Endocrinol
, vol.4
, pp. 75-82
-
-
Werder, E.A.1
Murset, G.2
Illig, R.3
-
24
-
-
0017754093
-
Rothmund-Thomson syndrome (poikiloderma congenitale) associated with mental retardation, growth disturbance, and skeletal features
-
Kassner EG, Qazi QH, Haller JO: Rothmund-Thomson syndrome (poikiloderma congenitale) associated with mental retardation, growth disturbance, and skeletal features. Skeletal Radiol 2:99-103, 1977.
-
(1977)
Skeletal Radiol
, vol.2
, pp. 99-103
-
-
Kassner, E.G.1
Qazi, Q.H.2
Haller, J.O.3
-
25
-
-
0017123406
-
Rothmund Thomson syndrome associated with osteosarcoma
-
Tokunaga M, Sato K, Funayama K: Rothmund Thomson syndrome associated with osteosarcoma. J Jpn Orthop Assoc 50:287-293, 1976.
-
(1976)
J Jpn Orthop Assoc
, vol.50
, pp. 287-293
-
-
Tokunaga, M.1
Sato, K.2
Funayama, K.3
-
26
-
-
0018120031
-
Increased excretion of urinary glycosaminoglycans in a case of Rothmund-Thomson
-
Tokunaga M, Wakamatsu E, Yosizawa Z: Increased excretion of urinary glycosaminoglycans in a case of Rothmund-Thomson. Tohoku J Exp Med 126:1-6, 1978.
-
(1978)
Tohoku J Exp Med
, vol.126
, pp. 1-6
-
-
Tokunaga, M.1
Wakamatsu, E.2
Yosizawa, Z.3
-
28
-
-
0022125921
-
Observation familiale de syndrome de Rothmund-Thomson: Observation en faveur de l'unicité du syndrome. Association à un ostéosarcome
-
Rebaud P, David L, Plauchu H: Observation familiale de syndrome de Rothmund-Thomson: Observation en faveur de l'unicité du syndrome. Association à un ostéosarcome. Pédiatric 6:487-492, 1985.
-
(1985)
Pédiatric
, vol.6
, pp. 487-492
-
-
Rebaud, P.1
David, L.2
Plauchu, H.3
-
30
-
-
0016537921
-
The Rothmund-Thomson syndrome
-
Diem E: The Rothmund-Thomson syndrome. Hautarzt 26:425-429, 1975.
-
(1975)
Hautarzt
, vol.26
, pp. 425-429
-
-
Diem, E.1
-
31
-
-
17344385250
-
Rothmund-Thomson syndrome and malignant disease
-
Davies MG: Rothmund-Thomson syndrome and malignant disease. Clin Exp Dermatol 7:455-457, 1982.
-
(1982)
Clin Exp Dermatol
, vol.7
, pp. 455-457
-
-
Davies, M.G.1
-
32
-
-
0021984739
-
Non-dermatological complications and genetic aspects of the Rothmund-Thomson syndrome
-
Starr DG, McClure JP, Connor JM: Non-dermatological complications and genetic aspects of the Rothmund-Thomson syndrome. Clin Genet 27:102-104, 1985.
-
(1985)
Clin Genet
, vol.27
, pp. 102-104
-
-
Starr, D.G.1
McClure, J.P.2
Connor, J.M.3
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