Lines of Blaschko

Journal of the American Academy of Dermatology

Volumn 31, Issue 2, 1994, Pages 157-190

  Orlow, Seth J ^a   Glick, Sharon A ^a  

^a NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOIDOSIS; ARTICLE; BASAL CELL NEVUS SYNDROME; CALCIFYING CHONDRODYSTROPHY; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; DARIER DISEASE; DYSOSTOSIS; GOLTZ SYNDROME; HUMAN; HYPERKERATOSIS; HYPERPIGMENTATION; HYPOHIDROTIC ECTODERMAL DYSPLASIA; INCONTINENTIA PIGMENTI; LICHEN PLANUS; MENKES SYNDROME; MUCINOSIS; MYCOSIS FUNGOIDES; POROKERATOSIS MIBELLI; PRIORITY JOURNAL; PSORIASIS; SEBACEOUS NEVUS; SKIN DISEASE;

FEMALE; GERMANY; HISTORY OF MEDICINE, 20TH CENT.; HUMAN; MALE; SKIN; SKIN DISEASES; SKIN NEOPLASMS; SUPPORT, NON-U.S. GOV'T;

EID: 0028108256     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0190-9622(94)70143-1     Document Type: Article

References (429)

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10. Wallace's line
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12. Tension lines, cleavage lines and hair tracts in man
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14. Absence de bipolarité dans les lignes de Blaschko
15. Oral mucosal involvement in nevus unius lateris (ichthyosis hystrix): a review of the literature and report of a case
16. L’analogie des lignes de Blaschko à l’oeil
17. Partial expression of sex-linked recessive amelogenesis imperfecta in females compatible with the Lyon hypothesis
18. X-linked ocular albinism: characteristic pattern of affection in female carriers
19. Iris pigment mosaicism in carriers of X-linked ocular albinism cum pigmento
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21. Sectorial cataract: a possible example of lyonisation
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31. Incontinentia pigmenti: a world statistical analysis
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33. Depigmented lesions in incontinentia pigmenti: a useful diagnostic sign
34. Anhidrotic and achromians lesions in incontinentia pigmenti
35. Focal dermal hypoplasia syndrome: an update
36. Focal dermal hypoplasia in a 46 X,Y male
37. Striation of bones in focal dermal hypoplasia: manifestation of functional mosaicism
38. Focal dermal hypoplasia (Goltz syndrome) in a male: a case report
39. Cutaneous defects of focal dermal hypoplasia: an ectomesodermal dysplasia syndrome
40. Focal dermal hypoplasia with keratoconus, papillomatosis of the esophagus and hydrocystomas
41. Focal dermal hypoplasia with apocrine nevi and striation of bones
42. A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration
43. Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase
44. Menkes kinky hair syndrome: an inherited defect in copper absorption with widespread effects
45. Pili torti as marker for carriers of Menkes disease
46. Menkes X-linked disease: two clonal cell populations in heterozygotes
47. Menkes kinky hair syndrome in a black infant
48. Maladie de Menkes: anomalie particulière de la pigmentation chez la mère et trois soeurs
49. Ectodermal dysplasia
50. Ectodermal dysplasias: some recollections and a classification
51. The ectodermal dysplasias: problems of classification and some newer syndromes
52. Multiple talgdrüsenhyperplasien bei X-chromosomaler hypohidrotischer ektodermaler dysplasie
53. Sweat pore counts in ectodermal dysplasias
54. Manifestation of the lines of Blaschko in women heterozygous for X-linked hypohidrotic ectodermal dysplasia
55. A typical case of X-linked anhidrotic ectodermal dysplasia and a diagnosis of carriers
56. Identification of functioning sweat pores and visualization of skin temperature patterns in X-linked hypohidrotic ectodermal dysplasia by whole body thermography
57. X-linked dominant chondrodysplasia punctata: review of literature and report of a case
58. X-linked dominant Conradi-Hünermann syndrome presenting as congenital erythroderma
59. Chondrodysplasia punctata: Conradi-Hünermann syndrome
60. Histologic and ultrastructural features of the ichthyotic skin in X-linked dominant chondrodysplasia punctata
61. Skin manifestations of Conradi’s disease
62. Acute skin manifestations of Conradi-Hüenermann syndrome in a male adult
63. Peroxisomal enzyme deficiency in X-linked dominant Conradi-Hünermann syndrome
64. Normal peroxisomal function and absent skeletal manifestations in Conradi-Hünermann syndrome
65. The CHILD syndrome: congenital hemidysplasia with ichthyosiform erythroderma and limb defects
66. X-chromosomal vertebrate Dermatosen
67. CHILD syndrom bei mutter and tochter
68. Ptychotropism as a cutaneous feature of the CHILD syndrome
69. CHILD naevus is not ILVEN [Letter]
70. Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome: case study and review of peroxisomal disorders in relation to skin disease
71. Possible new type of oral-facial-digital syndrome with retinal abnormalities: OFDS type (VIII)
72. Heterogeneity and variability in the oral-facial-digital syndromes
73. Polycystic kidneys, pancreatic cysts, and cystadenomatous bile ducts in the oral-facial-digital syndrome type I
74. Aplasia cutis congenita reminiscent of the lines of Blaschko
75. Familial cutaneous amyloidosis with systemic manifestations in males
76. X-linked cutaneous amyloidosis: further clinical and pathological observations
77. Macular amyloidosis simulating naevoid hyperpigmentation
78. Multiple endocrine neoplasia type 2a associated with cutaneous lichen amyloidosis
79. Familial lichen amyloidosis
80. Amyloidosis cutis: familial occurrence in three generations
81. Familial naevus sebaceus
82. Epidermal and other congenital organoid nevi
83. Darier-kóros eseteink genetilca és fejlödéstani elemzdse
84. Akanthokeratolytischer epidermaler nävus: Vererbbar ist die akanthokeratolyse, nicht der nävus
85. Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin
86. How many epidermal nevus syndromes exist?
87. Proteus syndrome: an expanded phenotype
88. Hypomelanosis of Ito: diagnostic criteria and report of 41 cases
89. Incontinentia pigmenti achromians (Ito)
90. Hypomelanosis of Ito
91. Congenital cranio-facial dysmorphosis associated with Ito’s syndrome (incontinentia pigmenti achromians): a case report
92. A malformation complex of ectrodactyly, clefting and hypomelanosis of Ito (incontinentia pigmenti achromians)
93. Chromosome mosaicism in hypomelanosis of Ito
94. Unusual brain MRI findings in a patient with hypomelanosis of Ito
95. Hypomelanosis of Ito [Letter]
96. Hypomelanosis of Ito associated with palmoplantar keratoderma and normal magnetic resonance imaging findings
97. Hypomelanosis of Ito (uncontinentia pigmenti achromians)
98. Hamartomatous dental cusps in hypomelanosis of Ito
99. Hypomelanosis of Ito
100. Systematized hypochromic nevus: incontunentia pigmenti achromians of Ito
101. Hypomelanosis of Ito (“incontinentia pigmenti achromians”)
102. Cytogenetic and dermatoglyphic findings in a familial case of hypomelanosis of Ito (incontinentia pigmenti achromians)
103. Ocular symptomatology in familial hypomelanosis of Ito
104. Hypomelanosis of Ito
105. Biology of hypopigmentation
106. Pigmentary demarcation lines: comparison of Negroes with Japanese
107. Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism
108. Hypomelanosis of Ito—a nonspecific marker of somatic mosaicism: report of case with trisomy 18 mosaicism
109. Hypomelanosis of Ito associated with benign tumors and chromosomal abnormalities: a neurocutaneous syndrome
110. Hypomelanosis of Ito: neurologic complications
111. Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito
112. Pigmentary dysplasias and chromosomal mosaicism: report of 9 cases
113. Hypomelanosis of Ito with trisomy 18 mosaicism
114. Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1
115. The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito
116. A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism
117. Hypomelanosis of Ito: association with a chromosomal abnormality
118. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci
119. Hypomelanosis of Ito associated with chromosomal translocation involving Xp11
120. Hypomelanosis of Ito in a girl with plexus papilloma and translocation (X;17)
121. Tentative assignment of hypomelanosis of Ito to 9q33→qter
122. Of mice, persons, and pigment [Editorial]
123. Hypomelanosis of Ito: involvement of chromosome aberrations in this syndrome
124. Linear and whorled nevoid hypermelanosis in a child with chromosomal mosaicism
125. Pigmentary dyspiasias, hypomelanosis of Ito, and genetic mosaicism
126. Genetic and congenital disorders
127. Unilateral systematized achromic naevus
128. Keratosis follicularis im bereich eines streifenformigen (systematisierten) naevus depigmentosus
129. Un caso di albanismo parziale
130. Congenital and non-congenital depigmentation
131. Congenital circumscribed hypomelanosis: a characterization based on electron microscopic study of tuberous sclerosis, nevus depigmentosus, and piebaldism
132. Population density of intraepidermal dendritic cells in nevus depigmentosus
133. Linear and whorled nevoid hypermelanosis
134. Linear and whorled nevoid hypermelanosis
135. Reticulate hyperpigmentation distributed in a zosteriform fashion: a new clinical type of hyperpigmentation
136. Zebra-like hyperpigmentation in an infant with multiple congenital defects
137. A case of reticulate hyperpigmentation distributed in a zosteriform fashion
138. A case of reticulate hyperpigmentation distributed in zosteriform fashion
139. Reticulate hyperpigmentation distributed in a zosteriform fashion [Letter]
140. Reticulate hyperpigmentation of Iijima, Naito, and Uyeno: a European case
141. Progressive zosteriform macular pigmented lesions [Letter]
142. Progressive cribiform and zosteriform hyperpigmentation
143. Bandes pigmentées atrophiques acquises suivant les lignes de Blaschko
144. Incontinentia pigmenti
145. Incontinentia pigmenti
146. Incontinentia pigmenti
147. Conjunctival and retinal incontinentia pigmenti
148. Incontinentia pigmenti
149. Encephalitis in two members of a family with incontinentia pigmenti (Bloch-Sulzberger syndrome)
150. Congenital pigmentation with atrophic scarring, associated with other congenital abnormalities
151. Incontinentia pigmenti
152. ? Incontinentia pigmenti
153. Incontinentia pigment (?) associated with hydrocephaly
154. Diffuse pigmentation, incontinentia pigmentia
155. Dermatose pigmentaire infantile réticulée: Forme particulière de l’incontinentia pigmenti?
156. Pigment anomalies of the skin in the human chimaera: their relation to systematized nevi
157. Genetic and developmental aspects of pathological pigmentation patterns
158. Chimerism, mosaicism and hybrids
159. Monozygotic twin girls with diploid/triploid chromosome mosaicism and cutaneous pigmentary dysplasia
160. Tnsomy 14 mosaicism in a 5 year old boy
161. Natural history of mosaic trisomy 14 syndrome
162. A live infant with trisomy 14 mosaicism and nuclear abnormalities of the neutrophils
163. Hypomelanosis of Ito: a cutaneous marker of chromosomal mosaicism [Abstract]
164. Hypomelanosis of Ito: spectrum of the disease
165. Birthmarks with serious medical significance: nevocellular nevi, sebaceous nevi, and multiple cafe au lait spots
166. Life history of organoid nevi: special reference to nevus sebaceus of Jadassohn
167. Jadassohn's naevus phakomatosis: 1. a report of two cases
168. Zur Kenntnis des Schimmelpenning-Feuerstein-Mims-Syndroms (Organoide naevus-phakomatose)
169. Nevus sebaceus associated with major ophthalmologic abnormalities
170. Linear nevus sebaceus with convulsions and mental retardation
171. Nevus sebaceus in association with an intracranial mass
172. Linear sebaceous nevus
173. Jadassohn's naevus phakomatosis: 2. a study based on a review of thirty-seven cases
174. Two unusual neurocutaneous disorders with facial cutaneous signs
175. Hypophosphatemic rickets/osteomalacia in linear sebaceous nevus syndrome: a variant of tumor-induced osteomalacia
176. Hypophosphatemic rickets in linear sebaceous nevus sequence
177. The epidermal nevus syndrome
178. Malignant neoplasms associated with nevus sebaceus of Jadassohn
179. Neurological involvement in nevus unis lateris and nevus linearis sebaceus
180. Wooly hair nevi with systematized linear epidermal naevus
181. The straight-hair nevus
182. Histopathologic varieties of epidermal nevus: a study of 160 cases
183. Vitamin-D resistant rickets associated with epidermal nevus syndrome: demonstration of a phosphaturic substance in the dermal lesions
184. Phakomatosis pigmentovascularis type IVa
185. Polyostotic fibrous dysplasia associated with extensive linear epidermal naevi
186. Albright's syndrome with rickets
187. Phakomatosis pigmentovasculanis type IIb with iris mammillations
188. Hereditary epidermolytic palmo-plantar keratoderma (Vörner type): report of a family and review of the literature
189. Nevus comedonicus with epidermolytic hyperkeratosis
190. Histopathologic concept of epidermolytic hyperkenatosis
191. Die granulöse degeneration bei naevus verrucosus bilatenalis: eine morphologische und funktionelle studie
192. Variations of congenital ichthyosiform erythroderma
193. Systematisienter naevus keratoticus (patientenvorstellung)
194. Bullous congenital ichthyosiform erythroderma
195. Érythrodermie ichtyosiforme congénitale bulleuse chez une file, naevus verruqueux épidermolytique chez son pène
196. Naevus verruqueux systématisé épidermolytique et érythrodermie ichtyosiforme congénitale bulleuse
197. Epidermolytic hyperkeratosis: generalized form in children from parents with systematized linear form
198. Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis
199. Nevoid follicular epidermolytic hyperkeratosis
200. Acrosyringial epidermolytic papulosis neviformis
201. Inflammatory linear verrucose epidermal nevus
202. Inflammatory linear verrucous epidermal nevus: report of seven cases and review of the literature
203. Epidermal nevi and the epidermal nevus syndrome
204. Analysis of epidermal fibrous proteins in inflammatory linear verrucous cpidermal nevus
205. Naevus épidermique verruqueux inflammatoire linéaire avec lésions achromiques
206. Inflammatory linear verrucous epidermal nevus: association with epidermal nevus syndrome
207. Inflammatory linear verrucous epidermal nevus (IL VEN) in a mother and her daughter
208. Linear porokeratosis: a distinctive clinical variant of porokeratosis of Mibelli
209. Pornkératose de Mibelli: forme systématisée hémicorporelle
210. Porokératose de Mibelli systématisée lichénoïde avec troubles pigmentaires et dégénérescence malpighienne spino-cellulaire
211. Ulcerative systematized porokeratosis (Mibelli)
212. Zosteriform porokeratosis: a report of two cases
213. Metastatic squamous cell carcinoma in linear porokeratosis of Mibelli
214. Porokeratosis (Mibelli): a case with extensive lesions
215. Linear porokeratosis in a 74-year-old woman
216. Disseminated superficial actinic porokeratosis: coexistence with other porokeratotic variants
217. Linear porokeratosis in two families with disseminated superficial actinic porokeratosis
218. Somatic recombination may explain linear porokeratosis associated with disseminated superficial actinic porokeratosis [Letter]
219. Porokeratosis: a mutant clonal keratosis of the epidermis. I. Histogenesis
220. Clonal chromosome abnormalities with preferential involvement of chromosome 3 in patients with porokeratosis of Mibelli
221. Porokératose de Mibelli linéaire chez des jumelles monozygotes
222. Nevus comedonicus: a review of the literature and report of twelve cases
223. Nevus comedonicus: a case with palmar involvement and review of the literature
224. Nevus comedonicus: report of three cases localized on glans penis
225. Treatment of nevus comedonicus with ammonium lactate lotion
226. Extensive nevus comedonicus
227. Nevus comedonicus: case report and brief review of the literature
228. Naevus unilateralis comedonicus: naevus follicularis keratosus of White
229. Nevus comedonicus bilateralis et verruciformis
230. Diffuse familial comedones
231. Generalized epidermolytic hyperkeratosis in the child of a parent with nevus comedonicus
232. The nevus comedonicus syndrome: a case report with emphasis on associated internal manifestations
233. Em heitreg zur klinik des naevus comedonicus
234. Unilateral cornedo nevus and cataract
235. Unpublished congenital dermatoocular syndrome (syndroma cataracto-comedonicum congenitale)
236. A newly recognized feature of ectrodactyly, ectodermal dysplasia, clefting (EEC) syndrome: comedone nevus
237. Naevus comedonicus unilateralis with partial Sturge-Weber syndrome and extensive vascular naevi with haemangiectatic hypertrophy of leg
238. Nevus cnmedonicus with epidermnlytic hyperkeratosis
239. Linear unilateral basal cell nevus with cnmednnes
240. Linear eccrine nevus with comedones
241. Naevus corniculatus: a new acantholytic disorder
242. Porokeratntic eccrine ostial and dermal duct nevus
243. Congenital unilateral punctate pcrokeratosis
244. Naevus folilcularis keratosus
245. Dramatic follicular plugging in pityriasis rubra pilaris
246. Pathogenesis of paraneoplastic follicular hyperkeratotic spicules in multiple myeloma
247. Syndrome paranéoplasique avec lésions papulo-kératosiques des extremités et kératose pilaire spinulosique diffuse
248. Paraneoplastic follicular hyperkeratosis responsive to etretinate
249. Unilateral systematized keratosis follicularis: a variant of Darier’s disease or an epidermal naevus (acantholytic dyskeratotic epidermal naevus)?
250. Morbus Darier zosteriformis
251. Dyskératose acantholytique régionale
252. A case of localized Darier's disease
253. Trichoepithelioma in a systematized epidermal nevus with acantholytic dyskeratosis
254. Unilateral keratosis follicularis
255. Zosteriform keratosis follicularis
256. Linear keratosis follicularis: A specific entity?
257. Naevus ou hamartome de Starink
258. Acantholytic dyskeratotic epidermal nacvus in a patient with guttate psoriasis on PUVA therapy
259. An acantholytic dyskeratotic epidermal naevus with other features of Darier's disease on the same side of the body
260. Enfermedad de Darier localizada: tratamiento tópico con ácido retinoico
261. A case of unilateral keratosis follicularis
262. Unilateral Daner's disease associated with Hodgkin's lymphoma
263. Nevo epidermico acantoiltico discheratosico a disposizione zonale
264. Localized Darier's disease: report of a case
265. A case of localized Darier's disease
266. Unilateral Darier's disease
267. Unilateral keratosis fofficularis: report of a case clinically resembling nevus unius latenis
268. Focal acantholytic dyskeratosis
269. Unilateral, linear, zosteriform epidermal nevus with acantholytic dyskeratosis
270. Danier's disease
271. Keratosis follicularis: report of a case with linear arrangement of lesions limited to the right lower extremity
272. Darier's disease resembling linear verrucous epidermal nevus
273. Keratosis follicularis unilateral type, nevoid distribution
274. Zosteriform keratosis follicularis treated topically with tretinoin
275. Zosteriform keratosis follicularis cleared with topically applied vitamin A acid
276. Relapsing linear acantholytic derinatosis
277. Deletion 3q27→3qter in an infant with mild dysmorphism, parietal meningocele, and neonatal miiaria rubra-like lesions
278. Deletioa 3q27→3qter associated with a new skin disorder?
279. Porokeratotic eccrine ostial and dermal duct naevus
280. Porokeratotic eccrine ostial and dermal duct nevus
281. Comedo naevus of the palm: a sweat duct naevus
282. Naevus sudoral eccrine palmaire pseudo-comédonien
283. Porokeratotic eccrine ostial and dermal duct nevus
284. Porokeratotic eccrine ostial and dermal duct nevus
285. Porokeratotic eccrine ostial and dermal duct nevus
286. Porokeratotic eccrine duct and hair follicle nevus
287. Porokeratotic eccrine ostial and dermal duct nevus: a case of systematized involvement
288. Unilateral, systematized, porokeratotic eccrine ostial and dermal duct aevi
289. Puzzling palmar and plantar papules
290. Puzzling palmar and plantar papules
291. Porokeratotic eccnine ostial and dermal duct nevus
292. Eccrine nevus with epidermal changes
293. Linear eccrine poroma
294. Unilateral linear nevoidal syningoma
295. Einseitige nävoide syringome
296. Eccrine syringofibroadenoma (Mascaró): an acrosyningeal hamartoma
297. Multiple linear spiradenomas
298. Zur histogenese der ekkrinen spiradenome
299. A zosteriform network of spiradenomas
300. Spiradenomi ecorini multipli a disposizione lineare
301. Multiple eklcrine spiradenome in streifenfdrmig navoider anordnung
302. Syringadenoma papilliferum
303. Life history of a naevus syringadenomatosus papilhiferus
304. Nevus sebaceus and syringocystadenoma papilliferum
305. Syringocystadenoma papilliferum in an unusual location
306. Linear papules on the neck of a child
307. Em fall von “adenoma fofficulare cutis papilliferum”
308. Segmental syringocystadenoma papilliferum in an unusual location
309. Syringocystadenoma papilliferum
310. Linear basal-cell naevos
311. Linear basal cell nevus
312. Linear unilateral basal cell nevus with comedo-like lesions
313. Unilateral linear basal cell nevus associated with diffuse osteoma cutis, unilateral anodontia, and abnormal bone mineralization
314. Linear unilateral basal cell nevus with comedones
315. Multiple superficial benign basal cell epithelionia of the skin
316. Linear unilateral basaloid follicular hamartoma
317. Basaloid follicular hamartoma: three cases with localized and systematized unilateral lesions
318. Unilateral skin lesions, cataracts, optic glioma and retardation: A variant of the epidermal nevus syndrome?
319. Quadrant distribution of basal cell nevi
320. Naevoid basal-cell carcinoma syndrome with unilateral neoplasms and pits
321. Nevoid basal cell carcinoma syndrome
322. Lichen striatus: a Blaschko linear acquired inflammatory skin eruption
323. Lichen striatus: epidemiologic study
324. A lichen stniatus—like eruption adopting the morphology of Blaschko lines
325. Le lichen striatus onychodystrophique: a propos de 4 cas avec revue de la litterature
326. Lichen striatus with onychodystrophy
327. Lichen stniatus: simultaneous occurrence in siblings
328. Blaschkite de l’adulte
329. Blaschkite de l’adulte
330. Un autre cas de Blaschkite chez l’adulte [Letter]
331. Blaschko-dermatitis: eine neue krankheit
332. Psoriasis zoniforme
333. Linear psoriasis
334. Naevus épidermique inflammatoire
335. Naevus épidermique verruqueux inflammatoire et linéafre
336. Inflammatory linear verrucose epidermal nevus
337. Inflammatory linear verrucose epidermal naevus
338. Psoriasis vulgaris et linearis
339. Psoriasis zosteriformis
340. Linear psoriasis
341. Case for diagnosis: Linear psoriasis?
342. Psoriasis and systematized epidenmal nevus
343. Systematized epidenmal nevus
344. Inflammatory linear verrucose epidermal naevus on linear psoriasis
345. Psoriasis ovenlying an epidermal nevus
346. Le psoriasis linéaire existe-t-il?
347. Dithranol in the treatment of inflammatory linear verrucous epidenmal nevus
348. Naevoid psoriasis
349. Congenital linear psoriasis: a case report
350. Somatic recombination may explain linear psoriasis
351. Zosteriform lichen planus
352. Lichen plan zoniforme
353. Lichen planus zoniformis
354. Deux cas de lichen plan a disposition zoniforme
355. A case of lichen planus lineanis: its relation to a cutaneous nerve experimentally shown
356. Discussion of case report of zosteriform lichen planus presented by JF Madison at Minnesota Dermatologic Society
357. Lichen planus verrucosus with zoster-like distribution
358. Linear lichen planus
359. The variations and course of lichen planus
360. Zosteriform lichen planus: case report
361. Lichen planus linearis: a case with an unusual zosteriform configuration
362. Differentiating vesicular linear lichen planus and lichen striatus
363. Unilateral lichen planus: an unusual presentation
364. Unilateral lichen planus
365. Ungewöhnlicher girlandenförmiger lichen planopilaris des Gesichtes
366. Linear lichen pianopilaris of the face
367. Lichenoid epidermal nevus: “linear lichen planus.”
368. Striärer lupus erythematodes im Verlauf der Blaschko-linien
369. Striärer lupus erythematodes im verlauf der Blaschko-linien [1. Steflungnahme] [Letter].
370. Lichen nitidus linéaire
371. Unilateral linear lichenoid eruption after bone marrow transplantation: An unmasking of tolerance to an abnormal keratinocyte clone?
372. Erythema dyschromicum perstans and lichen planus: Are they related?
373. Erythema dyschromicum perstans
374. Linear fixed drug eruption
375. Persistent papular plaques on the face
376. Linear alopecia mucinosa along Blaschko lines
377. Linear morphea with secondary cutaneous mucinosis
378. Cutaneous mucinosis of infancy: a congenital and linear variant
379. Hypopigmented mycosis fungoides: speculations about the mechanism of hypopigmentation
380. Clinical features and course of type A and type B vitiligo
381. Vitiligo in (apparent) dermatomal distribution
382. The McCune-Albright syndrome: a lethal gene surviving by mosaicism
383. Valeur diagnostique des taches café-au-lait (T.C.L.)
384. Melanotic macules in Albright's syndrome and neurofibromatosis
385. Linear arrangement of multiple congenital melanocytic nevi
386. Naevomatose juvénile de Spitz: forme profuse linéaire
387. Extensive blue nevus of Jadassohn-Tieche: report of case
388. Zosteriform lentiginous nevus
389. Naevus sur naevus: a propos de 7 observations, trois associées à d’autres dysplasies, et une à un mélanome malin invasif
390. Fatal melanoma arising in a zosteriform speckled lentiginous nevus
391. Widespread nevus spilus
392. Zosteriform lentiginous nevus
393. Multiple benign juvenile melanoma
394. Acquired linear dermal melanocytosis: nerve course distribution
395. Angiokeratoma corporis naeviforme
396. Verrucous hemangioma: a cmicopathologic study of 21 cases
397. Numerous papular glomus tumors localized on the abdomen: a report of a case and an ultrastructural study
398. Unilateral expression of multiple glomus tumors: an unusual occurrence
399. Unilateral dermatomal cavernous hemangiomatosis
400. Acquired zosteriform cavernous hemangiomas: brief clinical observation
401. Angioma serpiginosum
402. Chronic zosteriform eruption of the lower extremity
403. Chronic zosteriform eruption of the lower extremity
404. Maffuci’s syndrome (dyschondroplasia with hemangiomas): a case with early osseous changes
405. Unilateral nevoid telangiectasia: three new cases and the role of estrogen
406. Unilateral dermatomal superficial telangiectasia
407. Unilateral nevoid telangiectasia
408. Le trichodiscome de Pinkus
409. Linear and der matomal trichoepitheliomas
410. Hamartome infundibulopilaire linéaire avec dégénérescence basocellulaire
411. Zosteriformes xanthom
412. Verruciform xanthoma of the skin
413. Verruciform xanthoma in an epithelial news
414. Tumor conference #47: giant news lipomatosus
415. Linear pemphigus vulgaris after x-ray irradiation
416. Linear scieroderma: association with abnormalities of the spine and nervous system
417. Zur problematik des Becker-Nävus
418. Segmental neurofibromatosis
419. Segmentale neurofibromatose und keimbabnmosaik
420. Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin
421. Encephalocraniocutaneous lipomatosis
422. Encephalocraniocutaneous lipomatosis: a new neurocutaneous syndrome
423. Orbital cyst in addition to congenital cerebral and focal dermal malformations: a new entity
424. The oculocerebrocutaneous (Delleman) syndrome
425. Zosteriform leukaemia cutis
426. Early recognition and treatment of skin cancer
427. Self-Assessment examination answers
428. News angiolipomatosus vs focal dermalbypoplasia