Results 41 to 50 of about 77,663 (151)
The Concise Guide to PHARMACOLOGY 2025/26: Transporters
British Journal of Pharmacology, Volume 182, Issue S1, Page S404-S496, December 2025.The Concise Guide to Pharmacology 2025/26 marks the seventh edition in this series of biennial publications in the British Journal of Pharmacology. Presented in landscape format, the guide provides a comparative overview of the pharmacology of drug target families. The concise nature of the Concise Guide refers to the style of presentation, being clear,
Stephen P. H. Alexander +28 more
wiley +1 more source
Harlequin Ichthyosis: A Rare Case Report
, 2017 Harlequin fetus is a rare and the most severe genetic form of the congenital ichthyosis with an autosomal recessive inheritance. Incidence of the disease is nearly 1 in 3,00,000 live births.
Gallouj S +3 more
core +1 more source
A Case Report of Harlequin Ichtyosis
حیات, 2013 The harlequin fetus is the most severe type of congenital ichtyosis in which fetus suffers from chapped thick skin, abnormal face appearance, increased or decreased body temperature, respiratory distress, malnutrition, decreased sodium level, convulsion ...
Shahrbanoo Salehin +2 more
doaj
A Case Report of Harlequin Ichtyosis
حیات, 2012 The harlequin fetus is the most severe type of congenital ichtyosis in which fetus suffers from chapped thick skin, abnormal face appearance, increased or decreased body temperature, respiratory distress, malnutrition, decreased sodium level, convulsion ...
Shahrbanoo Salehin +2 more
doaj
Harlequin fetus – Icthyosis fetalis: Case report [PDF]
, 2021 We are presenting a newborn with a very rare and most severe form of congenital ichthyosis that is characterized by a thick, heavily keratinized and scaly skin.
Senai Sereke +2 more
openaire +1 more source
Ichthyosis Prematurity Syndrome: A Systematic Review of the Literature
Pediatric Dermatology, Volume 42, Issue 4, Page 747-753, July/August 2025.ABSTRACT Background/Objectives Ichthyosis prematurity syndrome (IPS) is a rare autosomal recessive congenital disorder characterized by premature birth, neonatal respiratory distress, eosinophilia, and a thick, clay‐like vernix at birth. This review aims to summarize the available reported cases of IPS, including genetic etiology, clinical features ...
Grace X. Li +3 more
wiley +1 more source
Archiv der Pharmazie, Volume 358, Issue 1, January 2025.Secondary metabolite profiles, phytocannabinoid, phenolic, and terpenoid profiles, and antiviral activity against SARS‐CoV‐2 of ethanolic extracts from nine Cannabis sativa L. genotypes were investigated, identifying distinct phytocannabinoid and phenolic components associated with the antiviral property and pharmacological profiles of the effective ...
Ermin Schadich +6 more
wiley +1 more source
گزارش 2 مورد جنين دلقکی(Harlequin Fetus) در 1 خانواده [PDF]
, 2005 (H.I)Harlequin Ichthyosis يک فرم شديد ايکتيوز اريترودرميک است که موجب می‌شود تا نوزاد ظاهر عجيب و منحصر به فردی در زمان تولد داشته باشد. ظاهر پوست و ماهيت کشنده بيماری سبب شده است تا تحت عنوان جنين دلقکی ( Harlequin Fetus ) نام‌گذاری شود اما از آن جا که ...
شکوهی, مریم +1 more
core
Romance in foreign accents: Harlequin-Mills & Boon in Australia
, 2009 This article is broadly interested in the adaptation and circulation of the mass-market romance genre as one example of the publishing industry’s production and distribution of cultural artefacts within and across national borders.
McWilliam, Kelly
core +1 more source
Pediatric Dermatology, Volume 41, Issue 6, Page 1106-1113, November/December 2024.ABSTRACT Background Focal dermal hypoplasia (FDH), also known as Goltz syndrome, is a rare ectodermal dysplasia that primarily affects the skin, skeleton, and eyes. It is an X‐linked dominant disorder, predominantly seen in females, caused by pathogenic variants in PORCN. Methods We characterized a case series of four genetically confirmed FDH patients
Laura Krogh Herlin +6 more
wiley +1 more source