BIOMAT Database Logo BIOMAT Database Logo

Prolonged coma and isoelectric electroencephalogram in a child with lysinuric protein intolerance. 1977

H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo

UI MeSH Term Description Entries
D008239 Lysine An essential amino acid. It is often added to animal feed. Enisyl,L-Lysine,Lysine Acetate,Lysine Hydrochloride,Acetate, Lysine,L Lysine
D008297 Male Males
D009952 Ornithine An amino acid produced in the urea cycle by the splitting off of urea from arginine. 2,5-Diaminopentanoic Acid,Ornithine Dihydrochloride, (L)-Isomer,Ornithine Hydrochloride, (D)-Isomer,Ornithine Hydrochloride, (DL)-Isomer,Ornithine Hydrochloride, (L)-Isomer,Ornithine Monoacetate, (L)-Isomer,Ornithine Monohydrobromide, (L)-Isomer,Ornithine Monohydrochloride, (D)-Isomer,Ornithine Monohydrochloride, (DL)-Isomer,Ornithine Phosphate (1:1), (L)-Isomer,Ornithine Sulfate (1:1), (L)-Isomer,Ornithine, (D)-Isomer,Ornithine, (DL)-Isomer,Ornithine, (L)-Isomer,2,5 Diaminopentanoic Acid
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D003128 Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION. Comatose,Pseudocoma,Comas,Pseudocomas
D004044 Dietary Proteins Proteins obtained from foods. They are the main source of the ESSENTIAL AMINO ACIDS. Proteins, Dietary,Dietary Protein,Protein, Dietary
D004569 Electroencephalography Recording of electric currents developed in the brain by means of electrodes applied to the scalp, to the surface of the brain, or placed within the substance of the brain. EEG,Electroencephalogram,Electroencephalograms
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000592 Amino Acid Metabolism, Inborn Errors Disorders affecting amino acid metabolism. The majority of these disorders are inherited and present in the neonatal period with metabolic disturbances (e.g., ACIDOSIS) and neurologic manifestations. They are present at birth, although they may not become symptomatic until later in life. Amino Acidopathies, Congenital,Amino Acid Metabolism Disorders, Inborn,Amino Acid Metabolism, Inborn Error,Amino Acid Metabolism, Inherited Disorders,Amino Acidopathies, Inborn,Congenital Amino Acidopathies,Inborn Errors, Amino Acid Metabolism,Inherited Errors of Amino Acid Metabolism,Amino Acidopathy, Congenital,Amino Acidopathy, Inborn,Congenital Amino Acidopathy,Inborn Amino Acidopathies,Inborn Amino Acidopathy
D001120 Arginine An essential amino acid that is physiologically active in the L-form. Arginine Hydrochloride,Arginine, L-Isomer,DL-Arginine Acetate, Monohydrate,L-Arginine,Arginine, L Isomer,DL Arginine Acetate, Monohydrate,Hydrochloride, Arginine,L Arginine,L-Isomer Arginine,Monohydrate DL-Arginine Acetate

Related Publications

H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Recovery from barbiturate overdose coma with a prolonged isoelectric electroencephalogram.
May 1968, Neurology,
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Lysinuric protein intolerance presenting as coma in a middle-aged man.
October 1996, The Western journal of medicine,
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Familial lysinuric protein intolerance presenting as coma in two adult siblings.
May 1989, Journal of neurology, neurosurgery, and psychiatry,
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
[Lysinuric protein intolerance].
November 1983, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde,
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Lysinuric protein intolerance.
January 1974, Birth defects original article series,
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Lysinuric protein intolerance.
September 1980, Lancet (London, England),
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Lysinuric protein intolerance.
November 1980, Lancet (London, England),
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Lysinuric protein intolerance.
May 1977, Annals of clinical biochemistry,
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Lysinuric protein intolerance.
August 1975, The American journal of medicine,
H Chan, and G J Billmeier, and S V Molinary, and H N Tucker, and B C Shin, and A Schaffer, and K Cavallo
Fanconi syndrome with lysinuric protein intolerance.
December 2014, Clinical kidney journal,
Copied contents to your clipboard!