-
1
-
-
0022655534
-
Aplasia cutis congenita: a clinical review and proposal for classification
-
Frieden I.J. Aplasia cutis congenita: a clinical review and proposal for classification. J. Am. Acad. Dermatol. 1986, 14:646-660.
-
(1986)
J. Am. Acad. Dermatol.
, vol.14
, pp. 646-660
-
-
Frieden, I.J.1
-
3
-
-
0016656139
-
Congenital midline scalp and skull defects
-
Lassman L.P., Sims D.G. Congenital midline scalp and skull defects. Arch. Dis. Child. 1950, 50:958-960.
-
(1950)
Arch. Dis. Child.
, vol.50
, pp. 958-960
-
-
Lassman, L.P.1
Sims, D.G.2
-
4
-
-
0015621279
-
Congenital absence of skin (aplasia cutis congenita)
-
Croce E.J., Purohit R.C., Janovski N.A. Congenital absence of skin (aplasia cutis congenita). Arch. Surg. 1973, 106:732-734.
-
(1973)
Arch. Surg.
, vol.106
, pp. 732-734
-
-
Croce, E.J.1
Purohit, R.C.2
Janovski, N.A.3
-
5
-
-
0036865524
-
Aplasia cutis congenita of the scalp
-
Martínez-Lage J.F., Almagro M.J., Hernández F.L., Poza M. Aplasia cutis congenita of the scalp. Childs Nerv. Syst. 2002, 18:634-637.
-
(2002)
Childs Nerv. Syst.
, vol.18
, pp. 634-637
-
-
Martínez-Lage, J.F.1
Almagro, M.J.2
Hernández, F.L.3
Poza, M.4
-
6
-
-
0001211649
-
Extrait d'une letter au sujet de trios enfants de la mĉme mère nés avec parties des extrémities dénuéé de peau
-
Cordon M. Extrait d'une letter au sujet de trios enfants de la mĉme mère nés avec parties des extrémities dénuéé de peau. J. Med. Chir. Pharm. 1767, 26:556-557.
-
(1767)
J. Med. Chir. Pharm.
, vol.26
, pp. 556-557
-
-
Cordon, M.1
-
7
-
-
42649089459
-
Aplasia cutis congenita of the scalp (5 observations)
-
Aloulou H., Chaari W., Khanfir S., Zroud N., Kammoun T.H., Abdelmoula M., Hachicha M. Aplasia cutis congenita of the scalp (5 observations). Arch. Pediatr. 2008, 15:382-387.
-
(2008)
Arch. Pediatr.
, vol.15
, pp. 382-387
-
-
Aloulou, H.1
Chaari, W.2
Khanfir, S.3
Zroud, N.4
Kammoun, T.H.5
Abdelmoula, M.6
Hachicha, M.7
-
8
-
-
0031865178
-
Extensive form of aplasia cutis congenital: a new syndrome
-
Park M.S., Hahn S.H., Hong C.H., Kim J.S., Kim H.S. Extensive form of aplasia cutis congenital: a new syndrome. J. Med. Genet. 1998, 35:609-611.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 609-611
-
-
Park, M.S.1
Hahn, S.H.2
Hong, C.H.3
Kim, J.S.4
Kim, H.S.5
-
9
-
-
40049098573
-
A case of systemic aplasia congenital: a newly recognized syndrome
-
Sugiura T., Kouwaki M., Kiyosawa S., Sasada Y., Maeda M., Goto K., Koyama N. A case of systemic aplasia congenital: a newly recognized syndrome. Eur. J. Pediatr. 2008, 167:409-413.
-
(2008)
Eur. J. Pediatr.
, vol.167
, pp. 409-413
-
-
Sugiura, T.1
Kouwaki, M.2
Kiyosawa, S.3
Sasada, Y.4
Maeda, M.5
Goto, K.6
Koyama, N.7
-
10
-
-
0029144784
-
Extensive symmetric truncal aplasia cutis congenital without fetus papyraceus or macroscopic evidence of placental abnormalities
-
Boente M.C., Frontini M.V., Acosta M.I., Saleme C., Barrionuevo S., Asial R. Extensive symmetric truncal aplasia cutis congenital without fetus papyraceus or macroscopic evidence of placental abnormalities. Pediatr. Dermatol. 1995, 12:228-230.
-
(1995)
Pediatr. Dermatol.
, vol.12
, pp. 228-230
-
-
Boente, M.C.1
Frontini, M.V.2
Acosta, M.I.3
Saleme, C.4
Barrionuevo, S.5
Asial, R.6
-
11
-
-
0017013615
-
Placental morphology in spontaneous human abortuses with normal and abnormal karyotypes
-
Honore L.H., Dill F.J., Foland B.J. Placental morphology in spontaneous human abortuses with normal and abnormal karyotypes. Teratology 2006, 14:151-166.
-
(2006)
Teratology
, vol.14
, pp. 151-166
-
-
Honore, L.H.1
Dill, F.J.2
Foland, B.J.3
-
13
-
-
0029040780
-
Aplasia cutis congenital and associated disorders: an update
-
Evers M.E., Steijlen P.M., Hamel B.C. Aplasia cutis congenital and associated disorders: an update. Clin. Genet. 1995, 47:295-301.
-
(1995)
Clin. Genet.
, vol.47
, pp. 295-301
-
-
Evers, M.E.1
Steijlen, P.M.2
Hamel, B.C.3
-
14
-
-
0028216223
-
Aplasia cutis congenita, elevated alpha-fetoprotein, and a distinct amniotic fluid acetylcholinesterase electrophoretic band
-
Dror Y., Gelman-Kohan Z., Hagai Z., Juster-Reicher A., Cohen R.N., Mogilmer B. Aplasia cutis congenita, elevated alpha-fetoprotein, and a distinct amniotic fluid acetylcholinesterase electrophoretic band. Am. J. Perinatol. 1994, 11:149-152.
-
(1994)
Am. J. Perinatol.
, vol.11
, pp. 149-152
-
-
Dror, Y.1
Gelman-Kohan, Z.2
Hagai, Z.3
Juster-Reicher, A.4
Cohen, R.N.5
Mogilmer, B.6
-
15
-
-
19544374472
-
Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy
-
Navarro C.L., De Sandre-Giovannoli A., Bernard R., Boccaccio I., Boyer A., Genevieve D., Hadj-Rabia S., et al. Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy. Hum. Mol. Genet. 2004, 13:493-503.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 493-503
-
-
Navarro, C.L.1
De Sandre-Giovannoli, A.2
Bernard, R.3
Boccaccio, I.4
Boyer, A.5
Genevieve, D.6
Hadj-Rabia, S.7
-
17
-
-
0026780634
-
Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature
-
Verloes A., Mulliez N., Gonzales M., Laloux F., Hermanns-Le T., Pierard G.E., et al. Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature. Am. J. Med. Genet. 1992, 43:539-547.
-
(1992)
Am. J. Med. Genet.
, vol.43
, pp. 539-547
-
-
Verloes, A.1
Mulliez, N.2
Gonzales, M.3
Laloux, F.4
Hermanns-Le, T.5
Pierard, G.E.6
-
19
-
-
57149100772
-
Johanson-Blizzard syndrome caused by identical UBR1 mutations in two unrelated girls, one with a cardiomyopathy
-
Elting M., Kariminejad A., de Sonnaville M.L., Ottenkamp J., Bauhuber S., Bozorgmehr B., et al. Johanson-Blizzard syndrome caused by identical UBR1 mutations in two unrelated girls, one with a cardiomyopathy. Am. J. Med. Genet. 2008, 146:3058-3061.
-
(2008)
Am. J. Med. Genet.
, vol.146
, pp. 3058-3061
-
-
Elting, M.1
Kariminejad, A.2
de Sonnaville, M.L.3
Ottenkamp, J.4
Bauhuber, S.5
Bozorgmehr, B.6
-
20
-
-
0031041675
-
Gastric outlet obstruction and epidermolysis bullosa
-
Shaw D.W., Fine J.D., Piacquadio D.J., Greenberg M.J., Wang-Rodriguez J., Eichenfield L.F., et al. Gastric outlet obstruction and epidermolysis bullosa. J. Am. Acad. Dermatol. 1997, 36:304-310.
-
(1997)
J. Am. Acad. Dermatol.
, vol.36
, pp. 304-310
-
-
Shaw, D.W.1
Fine, J.D.2
Piacquadio, D.J.3
Greenberg, M.J.4
Wang-Rodriguez, J.5
Eichenfield, L.F.6
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