-
3
-
-
0020608231
-
Epidermal Lipids, barrier function and desquamation
-
barrier function and desquamation. J Invest Dermatol 1983;80:44s-49s.
-
Elias P.M. Epidermal lipids, barrier function and desquamation. J Invest Dermatol 1983;80:44s-49s.
-
J Invest Dermatol
-
-
Elias, P.M.1
-
4
-
-
85035164196
-
Epidermal lipids and the biochemistry of keratinization
-
Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989:15-42.
-
Melnik B. Epidermal lipids and the biochemistry of keratinization. In: Traupe H. The Ichthvoses: A Guide to Clinical Diagnosis, Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989:15-42.
-
In: Traupe H. the Ichthvoses: A Guide to Clinical Diagnosis
-
-
Melnik, B.1
-
6
-
-
0342278149
-
Trophoblast sulphatase deficiency associated with X-chromosomal ichthyosis
-
van Duuren Chr Y, Vand de Vries GP, et al. 1976:120:180.
-
jobsis AC, van Duuren Chr Y, Vand de Vries GP, et al. Trophoblast sulphatase deficiency associated with X-chromosomal ichthyosis. Ned Tijdschr Geneeskd 1976:120:180.
-
Ned Tijdschr Geneeskd
-
-
Jobsis, A.C.1
-
7
-
-
85035159684
-
Steroid sulphatase deficiency and X-linked ichthyosis
-
Beaudet AL, Sly WS, Valle D, eds. Metabolic Basis of Inherited Disease. New York: McGraw-Hill, 1989;1945-64.
-
Shapiro LJ. Steroid sulphatase deficiency and X-linked ichthyosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. Metabolic Basis of Inherited Disease. New York: McGraw-Hill, 1989;1945-64.
-
In: Scriver CR
-
-
Shapiro, L.J.1
-
8
-
-
0017670083
-
Epidermal abnormalities in Refsum's disease
-
Marks R, Dykes PJ, Reynolds DJ. 1977;97:401-6.
-
Davies MG, Marks R, Dykes PJ, Reynolds DJ. Epidermal abnormalities in Refsum's disease. Br J Dermatol 1977;97:401-6.
-
Br J Dermatol
-
-
Davies, M.G.1
-
9
-
-
85035161986
-
Refsum's disease
-
Beaudet AL, Sly WS, Valle D, eds. Metabolic Basis of Inherited Disease. New York: McGraw-Hill, 1989:1533-50.
-
Steinberg D. Refsum's disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. Metabolic Basis of Inherited Disease. New York: McGraw-Hill, 1989:1533-50.
-
In: Scriver CR
-
-
Steinberg, D.1
-
10
-
-
0016612085
-
Neutral lipid storage disease: A new disorder of lipid metabolism
-
Patel A, Slavin G, Wills EJ, Andrews TM, Stewart Ci. 1975; 1:553-5.
-
Chanarin I, Patel A, Slavin G, Wills EJ, Andrews TM, Stewart Ci. Neutral lipid storage disease: A new disorder of lipid metabolism. Br MedJ 1975; 1:553-5.
-
Br MedJ
-
-
Chanarin, I.1
-
11
-
-
84991131535
-
Epidermal lipids
-
membranes and keratinization. 1981:20:1-19.
-
Elias PM. Epidermal lipids, membranes and keratinization. Int J Dermatol 1981:20:1-19.
-
Int J Dermatol
-
-
Elias, P.M.1
-
12
-
-
85035162889
-
The intercorneocyte space
-
Grayson S, Lampe MA, Williams ML, Brown BE. Plewig G, eds. Stratum Corneum. Heidelberg: Springer-Verlag, 1983;53-67.
-
Elias PM, Grayson S, Lampe MA, Williams ML, Brown BE. The intercorneocyte space. In: Marks R, Plewig G, eds. Stratum Corneum. Heidelberg: Springer-Verlag, 1983;53-67.
-
In: Marks R
-
-
Elias, P.M.1
-
13
-
-
85035160148
-
The ichthyoses
-
Elias PM. Dobson RL, eds. Pathogenesis of Skin Disease. New York: Churchill I.ivingstone, 1986:519-51.
-
Willimas ML, Elias PM. The ichthyoses. In: Thiers BH, Dobson RL, eds. Pathogenesis of Skin Disease. New York: Churchill I.ivingstone, 1986:519-51.
-
In: Thiers BH
-
-
Willimas, M.L.1
-
14
-
-
0028279523
-
Epidermal discase: Faulty keratin filaments take their toll
-
1994:6:6-7.
-
Compton JG. Epidermal discase: Faulty keratin filaments take their toll. Nat Genet 1994:6:6-7.
-
Nat Genet
-
-
Compton, J.G.1
-
15
-
-
84965266470
-
Clinical features of autosomal dominant and X-linked recessive ichthyosis in an English population
-
Kerr CB. 1966;1:947-50.
-
Wells RS, Kerr CB. Clinical features of autosomal dominant and X-linked recessive ichthyosis in an English population. Br Med J 1966;1:947-50.
-
Br Med J
-
-
Wells, R.S.1
-
16
-
-
84982077097
-
Geschlechtsgebundene Vererbung von Ichthyosis simplex (vulgaris) in einer schwedischen Bauernsippc
-
1927;8:45-8.
-
Lundborg H. Geschlechtsgebundene Vererbung von Ichthyosis simplex (vulgaris) in einer schwedischen Bauernsippc. Hereditas 1927;8:45-8.
-
Hereditas
-
-
Lundborg, H.1
-
17
-
-
0020615615
-
Clinical spectrum of steroid sulphatase deficiency: X-linked recessive ichthyosis
-
Happle R. birth complications and cryptorchidism. 1983; 140:19-21.
-
Traupe H, Happle R. Clinical spectrum of steroid sulphatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism. EurJ Pediatr 1983; 140:19-21.
-
EurJ Pediatr
-
-
Traupe, H.1
-
18
-
-
0022484659
-
Mechanisms in the association of cryptorchidism and X-linked recessive ichthyosis
-
Happle R. 1986:172:327-8.
-
Traupe H, Happle R. Mechanisms in the association of cryptorchidism and X-linked recessive ichthyosis. Dermatologica 1986:172:327-8.
-
Dermatologica
-
-
Traupe, H.1
-
19
-
-
0014401397
-
Eye changes in ichthyosis
-
Frost P, Weinstein G. 1968;206:2283-6.
-
Sever RJ, Frost P, Weinstein G. Eye changes in ichthyosis. JAMA 1968;206:2283-6.
-
JAMA
-
-
Sever, R.J.1
-
20
-
-
0021266564
-
Placental steroid sulfatase deficiency: Biochemical diagnosis and clinical review
-
Nielson MD, Lykkesfeldt AE. 1984:64:49-54.
-
Lykkesfeldt G, Nielson MD, Lykkesfeldt AE. Placental steroid sulfatase deficiency: Biochemical diagnosis and clinical review. Obstet Gynecol 1984:64:49-54.
-
Obstet Gynecol
-
-
Lykkesfeldt, G.1
-
21
-
-
0019510472
-
X-linked ichthyosis
-
1981;20:26-31.
-
Shapiro L. X-linked ichthyosis. Int J Dermatol 1981;20:26-31.
-
Int J Dermatol
-
-
Shapiro, L.1
-
22
-
-
84943725763
-
Familial X-linked ichthyosis
-
Allderdice PW, Shapiro LJ, Aveling J, Eales BA, Simms DJr. steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter. 1985;121:1524-8.
-
Ross JB, Allderdice PW, Shapiro LJ, Aveling J, Eales BA, Simms DJr. Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter. Arch Dermatol 1985;121:1524-8.
-
Arch Dermatol
-
-
Ross, J.B.1
-
23
-
-
0028114846
-
A clinical and genetic study of X-linked ichthyosis and contiguous gene defects
-
Emilion GG, Bouloux PMG, Harper JI. 1994;131:622-9.
-
Paige DG, Emilion GG, Bouloux PMG, Harper JI. A clinical and genetic study of X-linked ichthyosis and contiguous gene defects. Br J Dermatol 1994;131:622-9.
-
Br J Dermatol
-
-
Paige, D.G.1
-
24
-
-
0026550483
-
Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis
-
Grompe M, Parenti G, Yates J, Ballabio A. 1992:50:483-91.
-
Basier E, Grompe M, Parenti G, Yates J, Ballabio A. Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis. Am J Hum Genet 1992:50:483-91.
-
Am J Hum Genet
-
-
Basier, E.1
-
25
-
-
0019842473
-
Elias PM
-
Williams MI., X-linked ichthyosis and stratum corneum cell cohesion. Arch Dermatol 1981 ; 117:761-3.
-
Epstein EH Jr, Williams MI., Elias PM. Steroid sulfatase, X-linked ichthyosis and stratum corneum cell cohesion. Arch Dermatol 1981 ; 117:761-3.
-
Steroid Sulfatase
-
-
Epstein Jr., E.H.1
-
26
-
-
85142979119
-
-
Williams ML, Epstein EH Jr, law MYL, Fritsch PO, Elias PM. 1984;83:252-6.
-
Maloney ME, Williams ML, Epstein EH Jr, law MYL, Fritsch PO, Elias PM. I.ipids in the pathogenesis of ichthyosis: Topical cholesterol sulfate-induced scaling in hairless mice.J Invest Dermatol 1984;83:252-6.
-
I.ipids in the Pathogenesis of Ichthyosis: Topical Cholesterol Sulfate-induced Scaling in Hairless Mice.J Invest Dermatol
-
-
Maloney, M.E.1
-
27
-
-
0019783953
-
X-linked ichthyosis: Increased blood cholesterol sulfate and electrophoretic mobility of low density lipoprotein
-
Krauss RM, Shackleton CHL. 1981:214:659-60.
-
Epstein EH, Krauss RM, Shackleton CHL. X-linked ichthyosis: Increased blood cholesterol sulfate and electrophoretic mobility of low density lipoprotein. Science 1981:214:659-60.
-
Science
-
-
Epstein, E.H.1
-
28
-
-
0022390779
-
Das Klinische Bild der X-chromosomal-reJ.essiven Ichthyose
-
1985; 171:25-37.
-
Vo M. Das Klinische Bild der X-chromosomal-reJ.essiven Ichthyose. Dermatol Monatsschr 1985; 171:25-37.
-
Dermatol Monatsschr
-
-
Vo, M.1
-
29
-
-
0021185291
-
Autosoinal dominant lamellar ichthyosis: A new skin disorder
-
Kolde Ci, Happle R. 1984:26:457-61.
-
Traupe H, Kolde Ci, Happle R. Autosoinal dominant lamellar ichthyosis: A new skin disorder. Clin Genet 1984:26:457-61.
-
Clin Genet
-
-
Traupe, H.1
-
30
-
-
0028947560
-
Mutations of keratinocyte transglutaminase in lamellar ichthyosis
-
Rettier I, Bernascvoni K, et al. 1995:267:525-8.
-
Huber M, Rettier I, Bernascvoni K, et al. Mutations of keratinocyte transglutaminase in lamellar ichthyosis. Science 1995:267:525-8.
-
Science
-
-
Huber, M.1
-
31
-
-
0019391422
-
Sjôgren-I.arsson syndrome in Sweden
-
Gustavson KH, Holmgren G. genetical and epidemiological study. C'.lin Genet 1981:19:233-56.
-
Jagell S, Gustavson KH, Holmgren G. Sjôgren-I.arsson syndrome in Sweden. A clinical, genetical and epidemiological study. C'.lin Genet 1981:19:233-56.
-
A Clinical
-
-
Jagell, S.1
-
32
-
-
0002636920
-
Oligophrenia in combination with congenital ichthyosis and spastic disorders
-
Larsson T. 1957; 32(Suppl 113):1-113.
-
Sjôgren T, Larsson T. Oligophrenia in combination with congenital ichthyosis and spastic disorders. Acta Psychiatr Scand 1957; 32(Suppl 113):1-113.
-
Acta Psychiatr Scand
-
-
Sjôgren, T.1
-
34
-
-
0025649815
-
Depletion of alcohol (hexanol) dehydrogenase activity in the epidermis and jejunal mucosa in Sjogren-I.arsson syndrome
-
Lake BD, Smith W, Besley GTN, HarperJI. 1990; 95:632-4.
-
Judge MR, Lake BD, Smith W, Besley GTN, HarperJI. Depletion of alcohol (hexanol) dehydrogenase activity in the epidermis and jejunal mucosa in Sjogren-I.arsson syndrome. J Invest Dermatol 1990; 95:632-4.
-
J Invest Dermatol
-
-
Judge, M.R.1
-
35
-
-
0021288967
-
The Sjögren-Larsson syndrome
-
Jagell S. 1984:23:247-53.
-
Liden S, Jagell S. The Sjögren-Larsson syndrome. IntJ Dermatol 1984:23:247-53.
-
IntJ Dermatol
-
-
Liden, S.1
-
36
-
-
0015469025
-
Zur Kenntnis von Substrat und Bedeutung der sogenannten Schneckenspuren der Retina
-
1972:165:360-5.
-
Daicker B. Zur Kenntnis von Substrat und Bedeutung der sogenannten Schneckenspuren der Retina. Ophthalmologica 1972:165:360-5.
-
Ophthalmologica
-
-
Daicker, B.1
-
37
-
-
0014595755
-
Netherton's syndrome and ichthyosis linearis circumflexa
-
Stroud J. 1969; 100:550-8.
-
Altman J, Stroud J. Netherton's syndrome and ichthyosis linearis circumflexa. Arch Dermatol 1969; 100:550-8.
-
Arch Dermatol
-
-
Altman, J.1
-
38
-
-
0015022980
-
Réévaluation of ichthyosis and hair shaft abnormalities
-
Kirsch N, McGuireJ. 1971:103:266-71.
-
Hurwitz S, Kirsch N, McGuireJ. Réévaluation of ichthyosis and hair shaft abnormalities. Arch Dermatol 1971:103:266-71.
-
Arch Dermatol
-
-
Hurwitz, S.1
-
41
-
-
85035171280
-
The clinical spectrum of the Comèl-Netherton syndrome
-
Happle R. Genetic Counselling and Therapy. Heidelberg: SpringerVerlag, 1989:168-78.
-
Traupe H, Happle R. The clinical spectrum of the Comèl-Netherton syndrome. In: Traupe H. The Ichthyoses. A Guide to Clinical Diagnosis, Genetic Counselling and Therapy. Heidelberg: SpringerVerlag, 1989:168-78.
-
In: Traupe H. the Ichthyoses. A Guide to Clinical Diagnosis
-
-
Traupe, H.1
-
42
-
-
0028077645
-
A clinical and immunological study of Xethci ton's syndrome
-
Morgan G, Harper |I. 1994:131:615-21.
-
Judge MR, Morgan G, Harper |I. A clinical and immunological study of Xethci ton's syndrome. Br J Dennatol 1994:131:615-21.
-
Br J Dennatol
-
-
Judge, M.R.1
-
47
-
-
0014002385
-
Skin Manifestations of Conradi's Disease (Chondrodvsplasia Congenita Punclata).
-
Bodiam F.L. Skin manifestations of Conradi's disease (chondrodvsplasia congenita punclata). Arch Dennatol 1966;94:743-8.
-
(1966)
Arch Dennatol
, vol.94
, pp. 743-748
-
-
Bodiam, F.L.1
-
48
-
-
0018823632
-
Sex linked type of chondrodvsplasia punctata due to a new mutation
-
Hahedank M. 1979; 32:275-8.
-
Joosten R, Hahedank M. Sex linked type of chondrodvsplasia punctata due to a new mutation. Ada Pediatr Belg 1979; 32:275-8.
-
Ada Pediatr Belg
-
-
Joosten, R.1
-
49
-
-
0018611087
-
X-gekoppelt dominante chondrodvsplasia punctata
-
Kastner H. 1979:30:590-4.
-
Happle R, Kastner H. X-gekoppelt dominante chondrodvsplasia punctata. Ein osteokutanes Svndrom. Hautar/t 1979:30:590-4.
-
Ein Osteokutanes Svndrom. Hautar/t
-
-
Happle, R.1
-
53
-
-
0019462223
-
The keratitis
-
Greist MG, Norins AL. ichthyosis and deafness (KID) syndrome. 1981:117:285-9.
-
Skinner BA, Greist MG, Norins AL. The keratitis, ichthyosis and deafness (KID) syndrome. Arch Dermatol 1981:117:285-9.
-
Arch Dermatol
-
-
Skinner, B.A.1
-
54
-
-
0021629627
-
GilardiS
-
I. ewP.M, Saurat JH. ichthyosis and deafness and chronic mucocutaneous candidiasis: läse report and review of the literature. Pediatr Dermatol 1984:2:1-7.
-
Harms M.GilardiS, I. ewP.M, Saurat JH. KID svndrome (keralitis, ichthyosis and deafness) and chronic mucocutaneous candidiasis: (läse report and review of the literature. Pediatr Dermatol 1984:2:1-7.
-
KID Svndrome Keralitis
-
-
Harms, M.1
-
55
-
-
84943429907
-
Sauvan-Ferdani M
-
Breton A, Bonafé I., Bonerandi . ichthyosis and deafness (KID) svndrome. Vertical transmission and deatli from multiple squamous cell < arcinomas. Arch Dermatol 1987:123:777-82.
-
Gob JJ, Breton A, Bonafé [I., Sauvan-Ferdani M, Bonerandi [[. Keratitis, ichthyosis and deafness (KID) svndrome. Vertical transmission and deatli from multiple squamous cell < arcinomas. Arch Dermatol 1987:123:777-82.
-
Keratitis
-
-
Gob, J.J.1
-
56
-
-
0014292979
-
Eine weitere Form von atypische Erythrodermie mit Schwerhörigkeit und cerebraler Schädigung
-
Wissler H, Wendt GG. 1968:23:220-30.
-
Schnvder L'VV, Wissler H, Wendt GG. Eine weitere Form von atypische Erythrodermie mit Schwerhörigkeit und cerebraler Schädigung. Helv Pediatr Ada 1968:23:220-30.
-
Helv Pediatr Ada
-
-
Schnvder, L.V.V.1
-
57
-
-
0018751360
-
A congenital ichthvosiform syndrome with deafness and keratitis
-
Resneck JS, Jackson B. 1979:115:467-71.
-
Gram DL, Resneck JS, Jackson B. A congenital ichthvosiform syndrome with deafness and keratitis. Arch Dermatol 1979:115:467-71.
-
Arch Dermatol
-
-
Gram, D.L.1
-
59
-
-
0014785758
-
Histology of autosomal dominant ichthyosis vulgaris and X-linked ichthvosis
-
Ackerman AB, Ziprkowski L. 1971:101:524-7.
-
Feinstein A, Ackerman AB, Ziprkowski L. Histology of autosomal dominant ichthyosis vulgaris and X-linked ichthvosis. Arch Dermatol 1971:101:524-7.
-
Arch Dermatol
-
-
Feinstein, A.1
-
61
-
-
85035166811
-
Autosomal dominant ichthvosis vulgaris
-
Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989:45-53.
-
Traupe H. Autosomal dominant ichthvosis vulgaris. In: Traupe H. The Ichthvoses. A Guide to Clinical Diagnosis, Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989:45-53.
-
In: Traupe H. the Ichthvoses. A Guide to Clinical Diagnosis
-
-
Traupe, H.1
-
63
-
-
0026287604
-
Sweat gland function in patients with X-linked ichthyosis
-
De Ritis G, Fabbrocini G, Pi ocacdni EM, Illiano GM, Piccirillo A. 1991:82:677-8.
-
Delfino M, De Ritis G, Fabbrocini G, Pi ocacdni EM, Illiano GM, Piccirillo A. Sweat gland function in patients with X-linked ichthyosis. Recenti Prog Med 1991:82:677-8.
-
Recenti Prog Med
-
-
Delfino, M.1
-
64
-
-
85035162962
-
Variations ofcongenituicnthyosifomierythroderma
-
Pomeran/J. 1965;91:12K5.
-
Zeligman I, Pomeran/J. Variations ofcongenituicnthyosifomierythroderma. Arch Dennatol 1965;91:12(K5.
-
Arch Dennatol
-
-
Zeligman, I.1
-
66
-
-
0018089328
-
Epidermolytic hereditary palmoplantar keratoderma: Report of a family and treatment with oral aromatic retinoid
-
Höningsman H, aschke E. 1979:99:561-8.
-
Fritsch P, Höningsman H, [aschke E. Epidermolytic hereditary palmoplantar keratoderma: Report of a family and treatment with oral aromatic retinoid. Br J Dennatol 1979:99:561-8.
-
Br J Dennatol
-
-
Fritsch, P.1
-
67
-
-
0019458296
-
Nevus comedonicus with epidermolvtic hvperkeratosis: A report of four cases
-
Doyle JA, Winkelmann RK. 1981;117:86-8.
-
Bai sky S, Doyle JA, Winkelmann RK. Nevus comedonicus with epidermolvtic hvperkeratosis: A report of four cases. Arch Dermatol 1981;117:86-8.
-
Arch Dermatol
-
-
Bai Sky, S.1
-
69
-
-
0012265932
-
Histologie diagnosis of inflammatory skin diseases
-
1978:522,537,737.
-
Ackerman BA. Histologie diagnosis of inflammatory skin diseases. Philadelphia: Lea & Fehiger, 1978:522,537,737.
-
Philadelphia: Lea & Fehiger
-
-
Ackerman, B.A.1
-
70
-
-
85035164543
-
The epidermolytic (acanthokeratolytic) ichthyoses
-
Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989;139-53.
-
Traupe H. The epidermolytic (acanthokeratolytic) ichthyoses. In: Traupe H. The Ichthyoses. A Guide to Clinical Diagnosis, Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989;139-53.
-
In: Traupe H. the Ichthyoses. A Guide to Clinical Diagnosis
-
-
Traupe, H.1
-
72
-
-
0028012903
-
Prenatal diagnosis of epidermolytic hyperkeratosis by direct gene sequencing
-
Longley MA, Holder RA, Kuster W, Roop DR. 1994;102:13-16.
-
Rothnagel JA, Longley MA, Holder RA, Kuster W, Roop DR. Prenatal diagnosis of epidermolytic hyperkeratosis by direct gene sequencing. J Invest Dermatol 1994;102:13-16.
-
J Invest Dermatol
-
-
Rothnagel, J.A.1
-
73
-
-
0020692676
-
Epidermolytic hyperkeratosis: Ultrastructure and biochemistry of skin and amniotic fluid cells from two affected fetuses and a newborn infant
-
Dale BA, Sybert VP, Sagebiel RWC. 1983;80:222-7.
-
Holbrook KA, Dale BA, Sybert VP, Sagebiel RWC. Epidermolytic hyperkeratosis: Ultrastructure and biochemistry of skin and amniotic fluid cells from two affected fetuses and a newborn infant. J Invest Dermatol 1983;80:222-7.
-
J Invest Dermatol
-
-
Holbrook, K.A.1
-
74
-
-
0021922906
-
Heterogeneity in autosomal recessive ichthyosis: Clinical and biochemical differentiation of lamellar ichthyosis and nonbullous congenital ichthyosiform erythroderma
-
Elias PM. 1985;121:477-88.
-
Williams ML, Elias PM. Heterogeneity in autosomal recessive ichthyosis: Clinical and biochemical differentiation of lamellar ichthyosis and nonbullous congenital ichthyosiform erythroderma. Arch Dermatol 1985;121:477-88.
-
Arch Dermatol
-
-
Williams, M.L.1
-
75
-
-
0021992749
-
Clinical
-
Marks R. histological and cell kinetic discriminants between lamellar ichthyosis and non-bullous congenital ichthyosiform erythroderma. 1985;121:489-93.
-
Hazell M, Marks R. Clinical, histological and cell kinetic discriminants between lamellar ichthyosis and non-bullous congenital ichthyosiform erythroderma. Arch Dermatol 1985;121:489-93.
-
Arch Dermatol
-
-
Hazell, M.1
-
76
-
-
0013817263
-
Sjôgren-Larsson syndrome
-
Reed WB. 1965;92:545-52.
-
Heijer A, Reed WB. Sjôgren-Larsson syndrome. Arch Dermatol 1965;92:545-52.
-
Arch Dermatol
-
-
Heijer, A.1
-
78
-
-
0021921415
-
Ichthyosis Hnearis circumflexa: Morphological and biochemical studies
-
Manabe M, Negi M, Ogawa H. 1985; 112:277-83.
-
Yoshüke T, Manabe M, Negi M, Ogawa H. Ichthyosis Hnearis circumflexa: Morphological and biochemical studies. BrJ Dermatol 1985; 112:277-83.
-
BrJ Dermatol
-
-
Yoshüke, T.1
-
79
-
-
0016166357
-
Ichthyosis linearis circumflexa Cornel with trichorrhexis invaginata (Netherton's syndrome)
-
Frenk E. 1974;149:193-200.
-
Mevorah B, Frenk E. Ichthyosis linearis circumflexa Cornel with trichorrhexis invaginata (Netherton's syndrome). Alight microscopical study of skin changes. Dermatologica 1974;149:193-200.
-
Alight Microscopical Study of Skin Changes. Dermatologica
-
-
Mevorah, B.1
-
80
-
-
0021806009
-
Neutral lipid storage disease with ichthyosis: Defective lamellar body contents and intercellular dispersion
-
Williams ML. 1985;121:1000-8.
-
Elias PM, Williams ML. Neutral lipid storage disease with ichthyosis: Defective lamellar body contents and intercellular dispersion. Arch Dermatol 1985;121:1000-8.
-
Arch Dermatol
-
-
Elias, P.M.1
-
81
-
-
85035160354
-
X-linked dominant ichthyosis
-
Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989;179-86.
-
Traupe H. X-linked dominant ichthyosis. In: Traupe H. The Ichthyoses. A Guide to Clinical Diagnosis, Genetic Counselling and Therapy. Heidelberg: Springer-Verlag, 1989;179-86.
-
In: Traupe H. the Ichthyoses. A Guide to Clinical Diagnosis
-
-
Traupe, H.1
-
82
-
-
0021172213
-
Histological and ultrastructural features of the ichthyotlc skin in X-linked dominant chondrodysplasia punctata
-
Happle R. 1984;64:389-94.
-
Kolde G, Happle R. Histological and ultrastructural features of the ichthyotlc skin in X-linked dominant chondrodysplasia punctata. Acta Derm Venereol (Stockh) 1984;64:389-94.
-
Acta Derm Venereol (Stockh)
-
-
Kolde, G.1
-
83
-
-
0017763807
-
Ichthyosiform dermatosis
-
Alper JV. keratitis and deafness. 1977;i13:1701-14.
-
Baden HP, Alper JV. Ichthyosiform dermatosis, keratitis and deafness. Arch Dermatol 1977;i13:1701-14.
-
Arch Dermatol
-
-
Baden, H.P.1
-
84
-
-
0014495065
-
Carcinoma of the tongue in a child
-
Fournet BLF. 1969;27:269-70.
-
Lancaster L, Fournet BLF. Carcinoma of the tongue in a child. Report of a case. J Oral Surg 1969;27:269-70.
-
Report of A Case. J Oral Surg
-
-
Lancaster, L.1
-
86
-
-
0027376504
-
Prenatal diagnosis of genetic skin disease using fetal skin biopsy samples
-
Smith LT, Sherman E. 1993; 129:1437-54.
-
Holbrook KA, Smith LT, Sherman E. Prenatal diagnosis of genetic skin disease using fetal skin biopsy samples. Arch Dermatol 1993; 129:1437-54.
-
Arch Dermatol
-
-
Holbrook, K.A.1
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