𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A hepatorenal depressor reflex: A possible clue to the pathogenesis of the hepatorenal syndrome

✍ Scribed by Robert Safirstein; Marvin F. Levitt


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
205 KB
Volume
14
Category
Article
ISSN
0270-9139

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Splanchnic vasodilation and renal vasoco
✍ Jaime Bosch πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 399 KB

core region. The interrelations are formulated in Table 1. In the high replicative phase, the relatively higher expression of precore region than core gene results in translation of a greater amount of precore protein than core protein. The precore protein is then either secreted as HBeAg or transpo

Sensenbrenner syndrome: A new member of
✍ Marco Zaffanello; Francesca Diomedi-Camassei; Maria Luisa Melzi; Giuliano Torre; πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 292 KB πŸ‘ 2 views

## Abstract Cranioectodermal dysplasia (CED, Sensenbrenner syndrome; OMIM #218330) is an autosomal recessive disorder reported only in 15 cases, which is characterized by dolichocephaly, rhizomelic dwarfism, dental and nail dysplasia, and progressive tubulo‐interstitial nephritis (TIN) leading to e

Immunohistochemical distribution of rena
✍ Sugantha Govindarajan; Cynthia C. Nast; William L. Smith; Martin A. Koyle; Georg πŸ“‚ Article πŸ“… 1987 πŸ› John Wiley and Sons 🌐 English βš– 621 KB

To evaluate possible causes of the diminished prostaglandin production in advanced hepatorenal syndrome, prostaglandin endoperoxide synthase and prostacyclin synthase were localized and semiquantitated by immunofluorescence in postmortem, biopsy and nephrectomy renal tissues. In normal kidneys, anti

Fetal pads as a clue to the diagnosis of
✍ Daphne Lehalle; Charles Williams; Victoria Mok Siu; Jill Clayton-Smith πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 309 KB

Pitt-Hopkins syndrome (PHS) is characterized by severe mental retardation, characteristic facial features including a wide mouth and intermittent overbreathing. It is due to abnormalities of the TCF4 gene at 18q21.1 and over 50 cases have now been reported in the literature. The clinical features ov