Research Profile - College of Medicine and Health Science - United ...

Department of Pediatrics
Articles in Peerreviewed
Journals
Abdulrazzaq YM, Al Kendi A,
Nagelkerke N (2008). Child Care
Practice in the United Arab
Emirates: The ESACCIPS study. Acta
Paediatrica; 97: 590–595.
Abdulrazzaq YM, Moussa M,
Nagelkerke N (2008). National
Growth Charts for the United Arab
Emirates. Journal of
Epidemiology;18(6):295-303.
Abdulrazzaq YM, Osman N,
Kosanovic M, Adem A (2008). Trace
element content in plasma and
breast milk of well nourished
women. J Environ Sci Health 2008;
A43 (5):329-334.
Al-Gazali L, Hertecant J, Algawi K.,
El Teraifi H (2008). A new
autosomal recessive syndrome of
ocular colobomas. Ichhthyosis,
brain malformations and
endocrine abnormalities in an
inbred emirati family. Am J Med
Genet Part A, 146A:813-819.
Amirlak I, Al Dhaheri W, Narchi H
(2008). Dilated cardiomyopathy
secondary to nutritional rickets.
Ann Trop Paediatr., 28:227–230.
Amirlak I, Narchi H (2008). Isolated
orbital pseudotumor as the
presenting sign of systemic lupus
erythematosus. J Pediatr Ophthalmol
Strabismus, 45(1):51-54.
Brancati F,Travagilini L, Zablocka D,
Boltshauser E, Accorsi P, Montagna
G, Silhavy JL, Barrano G, Bertini E,
Emma F, Rigoli L, International JSRD
Study Group, Dallapiccola B,
Gleeson JG, Valente EM (2008).
RPGRIP1L mutations are mainly
associated with the cerebello-renal
phenotype of joubert syndrom –
related disorders. Clin Genet.,
74(2):164-170.
Cantegrel V, Silhavy JL, Bielas SL,
Swistun D, Marsh SE, Bertrand JY,
Attie-Bitach T, Holden KR, Dobyns
WB, Traver D, Al-Gazali L, Ali BR,
Linder TH, Caspary T, Otto EA,
Hildebrandt F, Gooding C, Johnson
CA, Bennett C, The International
Joubert Syndrome Related
Disorders (JSRD) Study Group,
Valente EM, Woods CG, Gleeson
JG (2008). Mutations in the cilia
gene ARL13B lead to Joubert
syndrome and related disorders.
Am J Hum Genet.,83(2):170-179.
Dawodu A, Bener A, Koutouby GA,
Varady E, Abdulrazzaq Y (2008).
Size at birth in a rapidly developing
economy: Intrauterine growth
pattern of UAE infants born to
healthy mothers. Annals of Human
Biology; 35(6): 615 – 623.
Hatchette T, Tipples G, Peters G,
Alsuwaidi A, Zhou J, Mailman T
(2008). Foscarnet Salvage Therapy
for Acyclovir-Resistant Varicella
Zoster: Report of a Novel
Thymidine Kinase Mutation and
Review of the Literature. Pediatric
Infectious Diseases Journal;27(1).
Khetyar M, Tinworth L, Syrris P,
Abushaban L, Abdulazzaq Y,
Silengo M, Carvalho J, Carter N
(2008). NKX2.5/NKX2.6 Mutations
are not a Common Cause of
Isolated Type 1 Truncus Arteriosus
in a Small Cohort of Multiethnic
Cases. Genet Test;12(4):467-469.
Kosanovic M, Adem A, Jokanovic
M, Abdulrazzaq YM (2008).
Simultaneous determination of
cadmium, mercury, lead, arsenic,
copper and zinc in human breast
milk by ICP-MS/microwave
digestion. Analytical Letters;
41(3):406 – 416.
Murthy SK, Malhotra AK, Jacob PS,
Naveed S, Al-Rowaished EEM, Mani
S, Padariyakam S, Pramathan R,
Lyndell S, Nath R, Ridha A, Al-Ali
MT, Al-Gazali L (2008). Anaploid
supernumerary marker
chromosome characterized by
array-CGH and FISH as inv dup
(3)(qter-q26.1::q26.1-qter) in a
child with dysmorphic features
and streaky pigmentation.
Molecular Cytogenetics, 1(1):19.
Narchi H, Al Marah M (2008). Does
vesicoureteral reflux increase
antibiotic resistance in pediatric
urinary tract infections. MAM.
Paediatrics me; 13 (4): 91-94.
Narchi H, Al-Hamdani M (2008).
First and recurrent pediatric
urinary tract infections: do they
have different antibiotic
susceptibilities” J Chemother,
20(4):472-7.
Narchi H, Basak R (2008). Bacterial
tracheitis- Not always primary. Turk
J Pediatr, 50: 409-411.
Narchi H, Donovan R (2008). Renal
power doppler ultrasound does
not predict renal scarring after
urinary tract infection. Scot Med J,
53(4):7-10.
Narchi H (2008). Assessment and
management of non-nephrotic
range proteinuria in children. Sri
Lanka Journal of Child Health; 37:
85-92.
Padmanabhan R, AbdulrazzaqYM,
Bastaki SMA, Shafiullah MM (2008).
Intrauterine Growth Restriction
and Skeletal Variations in Mouse
Fetuses Induced by Vigabatrin
Administered at Preimplantation
Stages of Development. Congenit
Anom;48(1):29-39.
Rauch A, Theil CT, Schindler D, Wick
U, Crow YJ, Ekici AB, van Essen Aj,
Goecke TO, Al-Gazali L,
Chrzanowska KH, Zweier C,
Brunner HG, Becker K, Curry CJ,
Dallapiccola B, Devriendt K, Dorfler
A, Kinning E, Megarbane A,
Meinecke P, Semple RK, Spranger
S, Toutain A, Trembath RC, VoB E,
Wilson L, Hennekam R, de Zegher
F, Dorr HG, Reis A (2008).
“Mutations in the pericentrin
(PCNT) gene cause primordial
dwarfism.”Science, 319(5864)816-
819.
Sasidharan P (2008). Evaluation
of Newborn Cyanosis. BMJ
Monograph, July 2008.
Sugimoto N, Rui T, Yang M,
Bharwani S, Handa O, Yoshida N,
Yoshikawa T, Kvietys PR (2008).
Points of control exerted along the
macrophage-endothelial cellpolymorphonuclear
neutrophil
axis by PECAM-1 in the innate
immune response of acute colonic
inflammation. J Immunol;
181(3):2145-54.
Suryadevara M, Schurman SJ,
Landas SK, Philip A, Gerlach CB,
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