Results 161 to 170 of about 115,827,059 (170)

Citrullinemia Type I in Chinese Children: Identification of Two Novel Argininosuccinate Synthetase Gene Mutations

Frontiers in Pediatrics, 2022
exaly  

EEG Changes During Recovery From Acute Severe Neonatal Citrullinemia

Electroencephalography and Clinical Neurophysiology, 1991
Robert R Clancy, R R Clancy
exaly  

Prenatal Diagnosis of Citrullinemia: Elevated Levels of Citrulline in the Amniotic Fluid in the Three Affected Pregnancies

Prenatal Diagnosis, 1984
M F Niermeijer, W Blom, J G M Huijmans
exaly  

Adult-Type Citrullinemia

Acta Neuropathologica, 1989
Riki Okeda
exaly  

Improving the Prenatal Diagnosis of Citrullinemia Using Citrulline/Ornithine+Arginine Ratio in Amniotic Fluid

Prenatal Diagnosis, 2002
P Kamoun, D Rabier, J Bardet
exaly  

A citrullinemia type 1 patient with a novel mutation in ASS1 gene

2016
Haberle, Johannes, ARSLAN, NUR, KÖSE, ENGİN   +2 more
openaire   +1 more source

Citrullinemia type 1 and its relationship to attention deficit hyperactivity disorder (ADHD)

Altable, Marcos, Akram, Muhammad, Msc, Emilio Díaz-Moreno   +2 more
openaire   +1 more source

Citrullinemia type 1 during pregnancy: A case study of nutritional management and supplementation

Molecular Genetics and Metabolism
T. Setlock, S.E. McCandless, M. Putra
openaire   +1 more source

BLOOD AMMONIA AS EARLY PREDICTOR OF CITRULLINEMIA TYPE 1 IN NEW BORN – A RARE CASE REPORT

INTERNATIONAL JOURNAL OF MEDICAL BIOCHEMISTRY
Vijayakumar. P. G, Seethalakshmi. S, Lakshmi. V, Rekha Sridhar   +3 more
openaire   +1 more source

S4579 Familial Hyperammonemia Requiring Liver Transplantation: A Case Series of Type 1 Citrullinemia

American Journal of Gastroenterology
Zehra Naseem, Amala J. Alenchery, Kadakkal Radhakrishnan, Sobia Laique   +3 more
openaire   +1 more source