Results 11 to 20 of about 17,809 (262)
A Case Report of Dyschromatosis Universalis Hereditaria (DUH) with Primary Ovarian Failure (POF) [PDF]
Dyschromatosis Universalis Hereditaria (DUH) belongs to a group of congenital diffuse reticulate pigmentary disorders characterised by both hypo and hyper pigmented macules. It is both hereditary and sporadic.
N.S Jayanthi +4 more
doaj +2 more sources
Review of Kozlovskyi, V. (2023). Kantian Anthropology. Sources. Constellations. Models. Kyiv: Duh i Litera.
Vlada Davidenko
semanticscholar +1 more source
Review of Tehilim. (2020). Tehilim - Psalms. Commentary by Rabbi Shimshon Raphael Hirsch (Vol. 1-2). Kyiv: Duh i Litera.
V. Kuznetsov
semanticscholar +1 more source
Jedna je od temeljnih čovjekovih odrednica ta da je obrazovljivo biće. Razlog tomu filozofijska tradicija nalazi u njegovoj duhovnoj duši. Za Humboldta je i njegovu obnovu sveučilišta, primjerice, duša osnova ovoga procesa.
Stjepan Radić
semanticscholar +1 more source
Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria
Background Dyschromatosis universalis hereditaria (DUH) is a pigmentary dermatosis characterized by generalized mottled macules with hypopigmention and hyperpigmention. ABCB6 and SASH1 are recently reported pathogenic genes related to DUH, and the aim of
Lu Cao +12 more
doaj +1 more source
A time-varying distributed unit hydrograph method considering soil moisture [PDF]
The distributed unit hydrograph (DUH) method has been widely used for flow routing in a watershed because it adequately characterizes the underlying surface characteristics and varying rainfall intensity.
B. Yi +14 more
doaj +1 more source
Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria. [PDF]
As a genetic disorder of abnormal pigmentation, the molecular basis of dyschromatosis universalis hereditaria (DUH) had remained unclear until recently when ABCB6 was reported as a causative gene of DUH.We performed genome-wide linkage scan using ...
Hong Liu +36 more
doaj +1 more source
Ultrasound reliability in detection of retinal tear in acute symptomatic posterior vitreous detachment with vitreous hemorrhage [PDF]
Cross-sectional study of 75 consecutive patients presenting with acute symptomatic posterior vitreous detachment (ASPVD) and vitreous hemorrhage was conducted at University Eye Clinic, University Hospital “Sveti Duh”, Zagreb, Croatia. To check ultrasound
Biljana Kuzmanović Elabjer +5 more
doaj +1 more source
Escherichia coli: a rare cause of meningitis in immuno-competent adult
A 35-year-old male of Asian ethnicity presented with complaints of high-grade fever, severe headache, vomiting, generalized seizures, deteriorated conscious level and neck stiffness.
Maryam Zafar +7 more
doaj +1 more source
Congenital Long QT Syndrome: a Systematic Review
Congenital long QT syndrome (LQTS) is a disorder of myocardial repolarization defined by a prolonged QT interval on electrocardiogram (ECG) that can cause ventricular arrhythmias and lead to sudden cardiac death.
Edvard Galić +7 more
doaj +1 more source

