X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (239) 239
index medicus (229) 229
male (144) 144
ichthyosis (112) 112
female (108) 108
dermatology (94) 94
child (64) 64
ichthyosis - genetics (64) 64
adult (61) 61
ichthyosis - complications (57) 57
infant, newborn (47) 47
adolescent (46) 46
child, preschool (43) 43
mutation (42) 42
x-linked ichthyosis (42) 42
infant (41) 41
skin (40) 40
pediatrics (37) 37
ichthyosis, x-linked - genetics (34) 34
ichthyosis - diagnosis (32) 32
ichthyosis, x-linked - complications (31) 31
pedigree (31) 31
ichthyosis - pathology (30) 30
diagnosis (29) 29
abridged index medicus (28) 28
lamellar ichthyosis (28) 28
syndrome (27) 27
genetics & heredity (26) 26
pregnancy (26) 26
steryl-sulfatase (26) 26
care and treatment (24) 24
genetic aspects (23) 23
genetic disorders (23) 23
middle aged (23) 23
mutations (23) 23
x chromosome (21) 21
phenotype (19) 19
skin - pathology (19) 19
steroid sulfatase (19) 19
risk factors (18) 18
skin diseases (18) 18
animals (17) 17
ichthyosis - drug therapy (16) 16
sulfatases - deficiency (16) 16
dermatology & venereal diseases (15) 15
gene deletion (15) 15
harlequin ichthyosis (15) 15
alopecia (14) 14
article (14) 14
diagnosis, differential (14) 14
steroid sulfatase deficiency (14) 14
analysis (13) 13
deficiency (13) 13
disease (13) 13
genetics (13) 13
medicine & public health (13) 13
ophthalmology (13) 13
erythroderma (12) 12
gene (12) 12
genes, recessive (12) 12
prenatal-diagnosis (12) 12
cell biology (11) 11
congenital ichthyosis (11) 11
genetic linkage (11) 11
ichthyosis - classification (11) 11
mental-retardation (11) 11
netherton-syndrome (11) 11
placenta - enzymology (11) 11
research (11) 11
aged (10) 10
children (10) 10
chromosome (10) 10
congenital diseases (10) 10
deletion (10) 10
disorders (10) 10
ichthyosis, x-linked - diagnosis (10) 10
skin diseases - genetics (10) 10
steryl-sulfatase - genetics (10) 10
young adult (10) 10
alopecia - complications (9) 9
arylsulfatases - genetics (9) 9
case studies (9) 9
complications and side effects (9) 9
cryptorchidism (9) 9
ectropion (9) 9
endocrinology & metabolism (9) 9
genes (9) 9
genodermatosis (9) 9
ichthyosis - therapy (9) 9
ichthyosis vulgaris (9) 9
ichthyosis, lamellar - diagnosis (9) 9
infants (9) 9
medicine (9) 9
molecular biology (9) 9
polymerase chain reaction (9) 9
prenatal diagnosis (9) 9
recessive congenital ichthyosis (9) 9
alopecia - genetics (8) 8
biochemistry (8) 8
consanguinity (8) 8
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, pp. e0164417 - e0164417
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 02/2016, Volume 13, Issue 2, pp. 1135 - 1140
Journal Article
Hinyokika kiyo. Acta urologica Japonica, ISSN 0018-1994, 11/2016, Volume 62, Issue 11, pp. 595 - 597
Steroid sulfatase (STS) deficiency is one of the causes of ichthyoses. STS genes on the X chromosome is responsible for this disease. Therefore, STS deficiency... 
Testicular Diseases - surgery | Humans | Child, Preschool | Ichthyosis, X-Linked - complications | Cryptorchidism | Male | Treatment Outcome | Testicular Diseases - etiology | Index Medicus
Journal Article
Journal Article
Journal Article
Journal Article
Clinical and Experimental Dermatology, ISSN 0307-6938, 01/2003, Volume 28, Issue 1, pp. 74 - 76
The association of recessive X‐linked ichthyosis (RXLI) and hypertrophic pyloric stenosis (HPS) has been considered to be due to a probable contiguous gene... 
DERMATOLOGY | Pyloric Stenosis - complications | Genes, Recessive - genetics | Pedigree | Humans | Ichthyosis, X-Linked - complications | Ichthyosis, X-Linked - genetics | Probability | Male | Pyloric Stenosis - genetics | Child | Hypertrophy | Index Medicus
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.