Supplemental Readings and References
697
P. A. Dennery, D. S. Seidman, and D. K. Stevenson: Neonatal Hyperbiliru-
binemia.
N ew E n g la n d J o u rn a l o f M ed icin e
344, 581 (2001).
C. Q. Edwards, L. M. Griffen, R. S. Ajioka, et al.: Screening for hemochro-
matosis: phenotype versus genotype.
S em in a rs in H em a to lo g y
35, 72
(1998).
G. H. Elder, R. J. Hift, and P. N. Meissner: The acute porphyrias.
L a n cet
349, 1613 (1997).
B. M. Gaston: Emissions testing for children, chapter 2: carbon monoxide.
J o u rn a l o f P ed ia trics
135, 537 (1999).
Y. Haimi-Cohen, P. Merlob, T. Marcus-Eidlits, et al.: Dubin-Johnson syn-
drome as a cause of neonatal jaundice: the importance of coporphyrins
investigation.
C lin ica l P ed ia trics
37, 511 (1998).
R. Kauppinen and P. Mustajoki: Prognosis of acute porphyria: occurrence
of acute attacks, precipitating factors, and associated diseases.
M ed icin e
71, 1 (1992).
Y. Maruo, H. Sato, T. Yamano, et al.: Gilbert syndrome caused by
a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-
glucuronyltransferase gene.
J o u rn a l o f P ed ia trics
132, 1045 (1998).
J. M. McCord: Iron: free radicals and oxidative injury.
S em in a rs in H e m a -
to lo g y
35,5 (1998).
G. Monaghan, A. McLellan, A. McGeehan, et al.: Gilbert’s syndrome is a
contributory factor in prolonged unconjugated hyperbilirubinemia of the
newborn.
J o u rn a l o f P ed ia trics
134,441 (1999).
E. Pollitt: Early iron deficiency anemia and later mental retardation.
A m e rica n J o u rn a l o f C lin ica l N u tritio n
69,4 (1999).
P. Ponka, C. Beaumont, and D. R. Richardson: Function and regu-
lation of transferrin and ferritin.
S em in a rs in H em a to lo g y
35, 35
(1998).
R. D. Press: Hemochromatosis: a simple “genetic” trait.
H o sp ita l P ra ctice
34,55(1999).
Report of a Meeting of Physicians and Scientists at the Royal Free Hos-
pital School of Medicine: Genetic hemochromatosis.
L a n c e t
349, 1688
(1997).
F. F. Rubaltelli, A. Novello, L. Zancan, et al: Serum and bile bilirubin
pigments in the differential diagnosis of Crigler-Najjar disease.
P ed ia trics
553,(1994).
A. Tefferl, L. Solberg, and R. Ellefson: Porphyrias: clinical evaluation
and interpretation of laboratory tests.
M a y o C lin ic P ro ceed in g s
69, 289
(1994).
C. G. Uasuf, A. Jatakanon, A. James, et al.: Exhaled carbon monoxide in
childhood asthma.
J o u rn a l o f P ed ia trics
135, 569 (1999).
J. N. Umbreit, M. E. Conrad, E. G. Moore, et al.: Iron absorption and cellular
transport: the mobilferrin/paraferritin paradigm.
S em in a rs in H em a to lo g y
35, 13(1998).
C. Utzel and M. E. Conrad: Absorption of heme iron.
S em in a rs in H e m a to l-
o g y
35, 27(1998).
previous page 729 Bhagavan Medical Biochemistry 2001 read online next page 731 Bhagavan Medical Biochemistry 2001 read online Home Toggle text on/off