-
1
-
-
0024239957
-
Cutis marmorata telangiectatica congenita: Clinicopathologic characteristics and differential diagnosis
-
Cohen PR, Zalar GL. Cutis marmorata telangiectatica congenita: clinicopathologic characteristics and differential diagnosis. Cutis 1988; 42: 518-22.
-
(1988)
Cutis
, vol.42
, pp. 518-522
-
-
Cohen, P.R.1
Zalar, G.L.2
-
2
-
-
0000445802
-
Über eine seltene angeborene Hautanomalie (Cutis marmorata telangiectatica congenita)
-
van Lohuizen CHJ. Über eine seltene angeborene Hautanomalie (Cutis marmorata telangiectatica congenita). Acta Derm Venereol (Stockh) 1922; 3: 202-11.
-
(1922)
Acta Derm Venereol (Stockh)
, vol.3
, pp. 202-211
-
-
Van Lohuizen, C.H.J.1
-
3
-
-
0027248564
-
Adams-Oliver syndrome: Cutis marmorata teleangiectatica congenita with multiple anomalies
-
Frank RA, Frosch PJ. Adams-Oliver syndrome: cutis marmorata teleangiectatica congenita with multiple anomalies. Dermatology 1993; 187: 205-8.
-
(1993)
Dermatology
, vol.187
, pp. 205-208
-
-
Frank, R.A.1
Frosch, P.J.2
-
4
-
-
3042798400
-
Generalized congenital phlebectasia
-
Humphries JM. Generalized congenital phlebectasia. J Pediatr 1952; 40: 486-8.
-
(1952)
J Pediatr
, vol.40
, pp. 486-488
-
-
Humphries, J.M.1
-
5
-
-
8044220620
-
Congenital generalized phlebectasia in a newborn
-
Bedell RF, Allison JR. Congenital generalized phlebectasia in a newborn. Arch Dermatol 1964; 90: 83-4.
-
(1964)
Arch Dermatol
, vol.90
, pp. 83-84
-
-
Bedell, R.F.1
Allison, J.R.2
-
6
-
-
0008211705
-
Congenital generalized phlebectasia
-
Kantor I, Yep D. Congenital generalized phlebectasia. Arch Dermatol 1966; 93: 774-5.
-
(1966)
Arch Dermatol
, vol.93
, pp. 774-775
-
-
Kantor, I.1
Yep, D.2
-
7
-
-
0000471024
-
Naevus vascularis reticularis (two cases)
-
Brain RT. Naevus vascularis reticularis (two cases). Proc R Soc Med 1954; 47: 172-3.
-
(1954)
Proc R Soc Med
, vol.47
, pp. 172-173
-
-
Brain, R.T.1
-
8
-
-
0001145798
-
Livedo reticularis. A review
-
Champion RH. Livedo reticularis. A review. Br J Dermatol 1965; 77: 167-79.
-
(1965)
Br J Dermatol
, vol.77
, pp. 167-179
-
-
Champion, R.H.1
-
9
-
-
0017694255
-
Cutis marmorata telangiectatica congenita (van Lohuizen's syndrome)
-
Dupont C. Cutis marmorata telangiectatica congenita (van Lohuizen's syndrome). Br J Dermatol 1977; 97: 437-9.
-
(1977)
Br J Dermatol
, vol.97
, pp. 437-439
-
-
Dupont, C.1
-
10
-
-
0019406954
-
Cutis marmorata telangiectatica with multiple congenital anomalies (van Lohuizen's syndrome)
-
Lee S, Lee JB, Kim JH et al. Cutis marmorata telangiectatica with multiple congenital anomalies (van Lohuizen's syndrome). Dermatology 1981; 163: 408-12.
-
(1981)
Dermatology
, vol.163
, pp. 408-412
-
-
Lee, S.1
Lee, J.B.2
Kim, J.H.3
-
11
-
-
0027191985
-
Cutis marmorata telangiectatica congenita: Long-term follow-up, review of the literature, and report of a case in conjunction with congenital hypothyroidism
-
Pehr K, Moroz B. Cutis marmorata telangiectatica congenita: long-term follow-up, review of the literature, and report of a case in conjunction with congenital hypothyroidism. Pediatr Dermatol 1993; 10: 6-11.
-
(1993)
Pediatr Dermatol
, vol.10
, pp. 6-11
-
-
Pehr, K.1
Moroz, B.2
-
12
-
-
0024432552
-
Cutis marmorata telangiectatica congenita with soft tissue herniations on the lower legs
-
Nicholls DSH, Harper JI. Cutis marmorata telangiectatica congenita with soft tissue herniations on the lower legs. Clin Exp Dermatol 1989; 14: 369-70.
-
(1989)
Clin Exp Dermatol
, vol.14
, pp. 369-370
-
-
Nicholls, D.S.H.1
Harper, J.I.2
-
13
-
-
0021367465
-
Congenital generalized fibromatosis: A review of the literature and report of a case associated with porencephaly, hemiatrophy, and cutis marmorata telangiectatica congenita
-
Spraker MK, Stack C, Esterly NB. Congenital generalized fibromatosis: a review of the literature and report of a case associated with porencephaly, hemiatrophy, and cutis marmorata telangiectatica congenita. J Am Acad Dermatol 1984; 10: 365-71.
-
(1984)
J Am Acad Dermatol
, vol.10
, pp. 365-371
-
-
Spraker, M.K.1
Stack, C.2
Esterly, N.B.3
-
14
-
-
0024370626
-
Cutis marmorata telangiectatica congenita: Report of 22 cases
-
Picascia DD, Esterly NB. Cutis marmorata telangiectatica congenita: report of 22 cases. J Am Acad Dermatol 1989; 20: 1098-104.
-
(1989)
J Am Acad Dermatol
, vol.20
, pp. 1098-1104
-
-
Picascia, D.D.1
Esterly, N.B.2
-
15
-
-
0021150408
-
Cutis marmorata telangiectatica congenita: Report of nine cases and review of the literature
-
Powell ST, Su WP. Cutis marmorata telangiectatica congenita: report of nine cases and review of the literature. Cutis 1984; 34: 305-12.
-
(1984)
Cutis
, vol.34
, pp. 305-312
-
-
Powell, S.T.1
Su, W.P.2
-
16
-
-
0025042775
-
Cutis marmorata telangiectatica congenita associated with bilateral congenital retinal detachment
-
Shields JA, Shields CL, Koller HP et al. Cutis marmorata telangiectatica congenita associated with bilateral congenital retinal detachment. Retina 1990 10: 135-9.
-
(1990)
Retina
, vol.10
, pp. 135-139
-
-
Shields, J.A.1
Shields, C.L.2
Koller, H.P.3
-
18
-
-
0027376218
-
Adams-Oliver syndrome: A case with juvenile chronic myelogenous leukemia and chylothorax
-
Farrell SA, Warda LJ, LaFlair P, Szymonowicz W. Adams-Oliver syndrome: a case with juvenile chronic myelogenous leukemia and chylothorax. Am J Med Genet 1993; 47: 1175-9.
-
(1993)
Am J Med Genet
, vol.47
, pp. 1175-1179
-
-
Farrell, S.A.1
Warda, L.J.2
LaFlair, P.3
Szymonowicz, W.4
-
19
-
-
0018501121
-
Cutis marmorata telangiectatica congenita and neonatal ascites
-
Schultz RB, Kocoshis S. Cutis marmorata telangiectatica congenita and neonatal ascites. J Pediatr 1979; 95: 157.
-
(1979)
J Pediatr
, vol.95
, pp. 157
-
-
Schultz, R.B.1
Kocoshis, S.2
-
20
-
-
0028130433
-
The causes and natural history of fetal ascites
-
Zelop C, Benacerraf BR. The causes and natural history of fetal ascites. Prenat Diagn 1994; 14: 941-6.
-
(1994)
Prenat Diagn
, vol.14
, pp. 941-946
-
-
Zelop, C.1
Benacerraf, B.R.2
-
21
-
-
0022355819
-
Aplasia cutis congenita: A report of 12 new families and review of the literature
-
Sybert VP. Aplasia cutis congenita: a report of 12 new families and review of the literature. Pediatr Dermatol 1985; 3: 1-14.
-
(1985)
Pediatr Dermatol
, vol.3
, pp. 1-14
-
-
Sybert, V.P.1
-
22
-
-
0023732558
-
Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): Report of ten cases and review of the literature
-
Küster W, Lenz W, Kääriäinen H, Majewski F. Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature. Am J Med Genet 1988; 31: 99-115.
-
(1988)
Am J Med Genet
, vol.31
, pp. 99-115
-
-
Küster, W.1
Lenz, W.2
Kääriäinen, H.3
Majewski, F.4
-
23
-
-
0023856210
-
Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome?
-
Toriello HV, Graff RG, Florentine MF et al. Scalp and limb defects with cutis marmorata telangiectatica congenita: Adams-Oliver syndrome? Am J Med Genet 1988; 29: 269-76.
-
(1988)
Am J Med Genet
, vol.29
, pp. 269-276
-
-
Toriello, H.V.1
Graff, R.G.2
Florentine, M.F.3
-
24
-
-
0025870339
-
Adams-Oliver syndrome revisited
-
Whitley CB, Gorlin RJ. Adams-Oliver syndrome revisited. Am J Med Genet 1991; 40: 319-26.
-
(1991)
Am J Med Genet
, vol.40
, pp. 319-326
-
-
Whitley, C.B.1
Gorlin, R.J.2
-
25
-
-
0342297253
-
Measurement of human chorionic gonadotrophin (hCG) as a screening test for Down's syndrome
-
(Grudzinskas JG, Chard T, Chapman M, Cuckle H, eds). Cambridge: Cambridge University Press
-
Chard T, Iles R. Measurement of human chorionic gonadotrophin (hCG) as a screening test for Down's syndrome. In: Screening for Down's Syndrome (Grudzinskas JG, Chard T, Chapman M, Cuckle H, eds). Cambridge: Cambridge University Press, 1994; 73-84.
-
(1994)
Screening for Down's Syndrome
, pp. 73-84
-
-
Chard, T.1
Iles, R.2
-
26
-
-
0027941823
-
Human maternal uniparental disomy for chromosome 16 and fetal development
-
Vaughan J, Ali Z, Bower S et al. Human maternal uniparental disomy for chromosome 16 and fetal development. Prenat Diagn 1994; 14: 751-6.
-
(1994)
Prenat Diagn
, vol.14
, pp. 751-756
-
-
Vaughan, J.1
Ali, Z.2
Bower, S.3
-
27
-
-
0027500471
-
Elevated human chorionic gonadotrophin levels in pregnancies with sex chromosome abnormalities
-
Barnes-Kedar I, Amiel A, Maor O et al. Elevated human chorionic gonadotrophin levels in pregnancies with sex chromosome abnormalities. Am J Med Genet 1993; 45: 356-7.
-
(1993)
Am J Med Genet
, vol.45
, pp. 356-357
-
-
Barnes-Kedar, I.1
Amiel, A.2
Maor, O.3
-
28
-
-
0028175584
-
Detection of fetal Turner syndrome with multiple-marker screening
-
Wenstrom KD, Williamson RA, Grant SS. Detection of fetal Turner syndrome with multiple-marker screening. Am J Obstet Gynecol 1994; 170: 570-3.
-
(1994)
Am J Obstet Gynecol
, vol.170
, pp. 570-573
-
-
Wenstrom, K.D.1
Williamson, R.A.2
Grant, S.S.3
-
29
-
-
0029165319
-
Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome
-
Benn PA, Horne D, Briganti BS, Greenstein RM. Prenatal diagnosis of diverse chromosome abnormalities in a population of patients identified by triple-marker testing as screen positive for Down syndrome. Am J Obstet Gynecol 1995; 173: 496-501.
-
(1995)
Am J Obstet Gynecol
, vol.173
, pp. 496-501
-
-
Benn, P.A.1
Horne, D.2
Briganti, B.S.3
Greenstein, R.M.4
-
30
-
-
0028343050
-
Multiple marker screen positivity in the presence of hydrops fetalis
-
Knowles S, Flett P. Multiple marker screen positivity in the presence of hydrops fetalis. Prenat Diagn 1994; 14: 403-5.
-
(1994)
Prenat Diagn
, vol.14
, pp. 403-405
-
-
Knowles, S.1
Flett, P.2
-
31
-
-
0026612103
-
Detection of hydatidiform mole in maternal serum screening programmes for Down's syndrome
-
Cuckle HS, Densem JW, Wald NJ. Detection of hydatidiform mole in maternal serum screening programmes for Down's syndrome. Br J Obstet Gynaecol 1992; 99: 495-7.
-
(1992)
Br J Obstet Gynaecol
, vol.99
, pp. 495-497
-
-
Cuckle, H.S.1
Densem, J.W.2
Wald, N.J.3
-
32
-
-
0028339575
-
Triploid partial molar pregnancy detected through maternal serum alpha-fetoprotein and hCG screening
-
Harper MA, Ruiz C, Pettenati MJ, Rao PN. Triploid partial molar pregnancy detected through maternal serum alpha-fetoprotein and hCG screening. Obstet Gynecol 1994; 83: 844-6.
-
(1994)
Obstet Gynecol
, vol.83
, pp. 844-846
-
-
Harper, M.A.1
Ruiz, C.2
Pettenati, M.J.3
Rao, P.N.4
|