Macedonian
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)

biliary atresia/seizures

Врската е зачувана во таблата со исечоци
НаписиКлинички испитувањаПатенти
13 резултати

Brachydactyly with extrahepatic biliary atresia, patent ductus arteriosus and seizures--a new syndrome?

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
Brachydactyly is a relatively common congenital anomaly and can be associated with many other malformations. However, brachydactyly in association with biliary atresia is rare. We present a male child with strikingly symmetrical brachydactyly and nail hypoplasia, extrahepatic biliary atresia, patent

Zimmermann-Laband syndrome in a child previously described with brachydactyly, extrahepatic biliary atresia, patent ductus arteriosus and seizures.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се

Pharmacokinetics of bupivacaine after continuous epidural infusion in infants with and without biliary atresia.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
BACKGROUND Continuous epidural infusion of bupivacaine is widely practiced for postoperative pain relief in pediatric patients. However, bupivacaine may induce adverse effects in infants (convulsions or cardiac arrhythmias), likely because of decreased hepatic clearance and serum protein binding

Neuromuscular complication after liver transplant in children: a single-center experience.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
OBJECTIVE Neurologic complications are a significant cause of morbidity in children after liver transplant. In this study, we sought to evaluate the neurologic complications in children after liver transplant. METHODS All children aged younger than 18 years old who had undergone liver transplant

Unusual clustering of diseases and manifestations in pediatric admissions of a tertiary care center.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
BACKGROUND Cluster investigations has been an important tool in investigations of diseases. While clustering of diseases or a manifestation in community can cause great public alarm, similar unexplained clustering in hospital admissions has baffled clinicians. OBJECTIVE (a) To determine whether

Neurologic complications of pediatric liver transplantation.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
The neurologic complications of 24 children, ages 5 months to 18 years, following orthotopic liver transplantation at the Indiana University hospitals are reported. Biliary atresia (14 patients) was the most common cause for orthotopic liver transplantation. Three children died. Seventeen children

The use of interferon for the treatment of viral hepatitis in pediatric liver transplant recipients.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
Between January 1990 and July 1992, 12 children with viral hepatitis occurring after liver transplantation (LTx) were treated with interferon alpha-2b. Seven were female and 5 were male; their ages ranged between 0.7 and 14.7 years (mean = 5.4 years). The indications for LTx included biliary atresia

Spontaneously ruptured choledochal cyst: Rare diagnosis on hepatic scintigraphy.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
A 47-day-old female infant presented with congenital inguinal hernia, seizure on the 2(nd) day of life, fever, progressive jaundice, acholic stools and distension of abdomen. She was suspected to have choledochal cyst with extrahepatic biliary atresia (EHBA) and referred for an Hepatobiliary Tc-99m

Experience with heart transplantation in children.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
Between March 1981 and March 1986, 200 orthotopic heart transplantations were performed at the University of Pittsburgh. Fourteen of those procedures were carried out in children 2 to 16 years of age. Two children received combined liver and heart transplants; one because of familial

Predictable and Unusual Adverse Effects of Immunosuppression in Pediatric Liver Transplant Patients.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
Our aim was to determine potentially adverse effects of immunosuppressive protocols after liver transplantation in children.The medical records of 60 children who underwent liver transplant retrospectively analyzed. Corticosteroid, tacrolimus, and

Transaminase in rotavirus gastroenteritis.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
BACKGROUND Children infected with rotavirus often show increased levels of transaminase, and symptoms are characterized by white stool, similar to biliary atresia. Rotavirus infections are also sporadically accompanied with convulsions, encephalopathy and Reye syndrome. The aim of the present study

Leukoencephalopathy syndrome after living-donor liver transplantation.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
OBJECTIVE Leukoencephalopathy syndrome is a neurologic complication after organ transplantation caused predominantly by the neurotoxic effects of immunosuppressive agents on cerebral white matter. We determined the incidence and features of leukoencephalopathy syndrome in recipients after

Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome.

Само регистрираните корисници можат да преведуваат статии
Пријавете се / пријавете се
Rare individuals with 20p11.2 proximal deletions have been previously reported, with a variable phenotype that includes heterotaxy, biliary atresia, midline brain defects associated with panhypopituitarism, intellectual disability, scoliosis, and seizures. Deletions have ranged in size from 277 kb
Придружете се на нашата
страница на Facebook

Најкомплетната база на податоци за лековити билки поддржана од науката

  • Работи на 55 јазици
  • Лекови од билки поддржани од науката
  • Препознавање на билки по слика
  • Интерактивна GPS мапа - означете ги билките на локацијата (наскоро)
  • Прочитајте научни публикации поврзани со вашето пребарување
  • Пребарувајте лековити билки според нивните ефекти
  • Организирајте ги вашите интереси и останете во тек со истражувањето на новостите, клиничките испитувања и патентите

Напишете симптом или болест и прочитајте за билки што можат да помогнат, напишете билка и видете болести и симптоми против кои се користи.
* Сите информации се базираат на објавени научни истражувања

Google Play badgeApp Store badge