X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1379) 1379
Publication (88) 88
Book Chapter (18) 18
Book Review (4) 4
Book / eBook (3) 3
Magazine Article (3) 3
Conference Proceeding (1) 1
Data Set (1) 1
Government Document (1) 1
Reference (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (952) 952
incontinentia pigmenti (860) 860
female (606) 606
male (299) 299
incontinentia pigmenti - genetics (283) 283
index medicus (253) 253
incontinentia pigmenti - pathology (223) 223
infant (220) 220
infant, newborn (219) 219
incontinentia pigmenti - diagnosis (199) 199
child (185) 185
dermatology (180) 180
genetics & heredity (173) 173
incontinentia pigmenti - complications (171) 171
pediatrics (163) 163
child, preschool (161) 161
adult (139) 139
mutation (137) 137
i-kappa b kinase - genetics (127) 127
animals (117) 117
nemo (107) 107
skin - pathology (106) 106
diagnosis, differential (104) 104
nf-kappa-b (100) 100
mosaicism (97) 97
x chromosome (97) 97
ophthalmology (86) 86
activation (84) 84
bloch-sulzberger syndrome (84) 84
pigmentation disorders (84) 84
skin (84) 84
adolescent (81) 81
biochemistry & molecular biology (81) 81
mice (81) 81
pedigree (80) 80
ectodermal dysplasia (72) 72
pigmentation disorders - genetics (71) 71
phenotype (69) 69
cell biology (67) 67
incontinentia pigmenti achromians (62) 62
pigmentation (62) 62
mutations (61) 61
gene (60) 60
immunology (60) 60
diagnosis (59) 59
nf-kappa b - metabolism (59) 59
clinical neurology (58) 58
magnetic resonance imaging (57) 57
genetic linkage (52) 52
signal transduction (52) 52
anhidrotic ectodermal dysplasia (51) 51
gamma-deficient mice (50) 50
immunodeficiency (50) 50
ectodermal dysplasia - genetics (47) 47
genetic aspects (47) 47
dermatology & venereal diseases (46) 46
hypomelanosis of ito (46) 46
biopsy (45) 45
middle aged (45) 45
hypohidrotic ectodermal dysplasia (44) 44
ikk-gamma (44) 44
karyotyping (44) 44
pigmentation disorders - pathology (44) 44
i-kappa b kinase (43) 43
congenital, hereditary, and neonatal diseases and abnormalities (42) 42
incontinentia pigmenti - physiopathology (42) 42
incontinentia-pigmenti (42) 42
skin and connective tissue diseases (42) 42
nf-kappa b (41) 41
fluorescein angiography (40) 40
immune-deficiency (40) 40
deficient mice (39) 39
disease (39) 39
nf-κb (39) 39
severe liver degeneration (39) 39
chromosome mapping (38) 38
i-kappa b kinase - metabolism (38) 38
kinase complex (38) 38
brain - pathology (37) 37
hypomelanosis (37) 37
dosage compensation, genetic (36) 36
ito (36) 36
pigmentation disorders - complications (36) 36
syndrome (36) 36
x-linked disorder (35) 35
apoptosis (34) 34
deletion (34) 34
genodermatosis (34) 34
inflammation (34) 34
molecular sequence data (34) 34
case report (32) 32
mutation - genetics (32) 32
skin diseases (32) 32
nf-kappa b - genetics (31) 31
gene deletion (30) 30
genetics (30) 30
medicine, research & experimental (30) 30
sense organs (30) 30
pregnancy (29) 29
follow-up studies (28) 28
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1138) 1138
French (71) 71
Spanish (54) 54
German (46) 46
Korean (21) 21
Portuguese (13) 13
Italian (12) 12
Japanese (8) 8
Polish (8) 8
Dutch (6) 6
Russian (6) 6
Chinese (4) 4
Turkish (4) 4
Norwegian (2) 2
Slovak (2) 2
Croatian (1) 1
Czech (1) 1
Greek (1) 1
Swedish (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Actas Dermo-Sifiliográficas (English Edition), ISSN 1578-2190, 05/2019, Volume 110, Issue 4, pp. 273 - 278
Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysplasia. It is an X-linked dominant disorder caused by mutations in the gene on... 
Clínica | Clinical features | Incontinentia pigmenti | Treatment | Diagnóstico | Tratamiento | Diagnosis | IKBKG/NEMO | Incontinencia pigmenti
Journal Article
Actas Dermo-Sifiliograficas, ISSN 0001-7310, 2019
Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysplasia. It is an X-linked dominant disorder caused by mutations in the... 
Clinical features | Incontinentia pigmenti | Treatment | Diagnosis | IKBKG/NEMO
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2019, Volume 179, Issue 8, pp. 1415 - 1419
Incontinentia Pigmenti (IP; MIM 308300) is an X‐linked dominant genodermatosis caused by pathogenic variant in IKBKG. The phenotype in adults is poorly... 
phenotype | Incontinentia Pigmenti | ectodermal dysplasia | IKBKG | adult | BLOCH-SULZBERGER | ACTIVATION | GENETICS & HEREDITY | Dysplasia | Adults | Skin | Market surveys | Cataracts | Dentures | Jaw | Phenotypes | Nails | Retina | Cognition | Polls & surveys | Genodermatosis | Intolerance | Surgery | Diagnosis | Microphthalmia
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 09/2016, Volume 33, Issue 5, pp. e280 - e281
Late recurrences of first‐stage inflammatory vesiculobullous lesions of incontinentia pigmenti (IP) are uncommon but have been reported to occur in the setting... 
PEDIATRICS | DERMATOLOGY | Incontinentia Pigmenti - diagnosis | Coxsackievirus Infections - diagnosis | Humans | Infant | Male | Coxsackievirus Infections - complications | Incontinentia Pigmenti - virology | Coxsackievirus infections
Journal Article
Kathmandu University Medical Journal, ISSN 1812-2027, 01/2013, Volume 11, Issue 41, pp. 91 - 93
Journal Article
Molecular Cell, ISSN 1097-2765, 2000, Volume 5, Issue 6, pp. 981 - 992
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 11/2018, Volume 176, Issue 11, pp. 2318 - 2324
Incontinentia Pigmenti (IP) is an X‐linked rare genodermatosis caused by mutations in the IKBKG gene, which is essential to NF‐κB pathway activation and thus... 
genodermatosis | incontinentia pigmenti | IKBKG | NEMO | REARRANGEMENT | GENETIC-BASIS | ALLELES | GENETICS & HEREDITY | MUTATIONS | EXPRESSION | Medicine, Experimental | Medical research | Genodermatosis | Incontinentia Pigmenti | IKBKG gene | Cell survival | Clonal deletion
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 03/2019, Volume 81, Issue 5, pp. 1142 - 1149
Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis that affects multiple systems with highly variable phenotypic expressivity. Although... 
Comparative analysis | Children's hospitals
Journal Article
Journal Article
European Journal of Pediatrics, ISSN 0340-6199, 8/2013, Volume 172, Issue 8, pp. 1137 - 1138
Incontinentia pigmenti (IP) is an uncommon X-linked dominant genodermatosis. It affects predominantly females and is lethal in utero in male fetuses. We herein... 
Medicine & Public Health | Pediatrics | Incontinentia pigmenti | PEDIATRICS | Incontinentia Pigmenti - genetics | Humans | Incontinentia Pigmenti - pathology | Genetic Diseases, X-Linked - pathology | Female | Infant | Infant, Newborn | Skin - pathology | Index Medicus
Journal Article