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Showing 10 out of a total of 81 results for collection: Pediatrics and Adolescent Medicine - Faculty Publications. (0.011 seconds)

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Epileptic and electroencephalographic manifestations of guanidinoacetate-methyltransferase deficiency

Mikati A.G.; Abu Gheida I.; Shamseddine A.; Mikati M.A.; Karam P.E. (MONTROUGE, 2013)
A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype

Sanjad S.A.; Hariri A.; Habbal Z.M.; Lifton R.P. (NEW YORK, 2007)
Exploring the characteristics of children with obstructive adenoid responding to mometasone fuorate monohydrate: Preliminary results

Bitar M.A.; Mahfoud L.; Nassar J.; Dana R. (NEW YORK, 2013)
The effect of vagus nerve stimulation therapy on body mass index in children

Kansagra S.; Ataya N.; Lewis D.; Gallentine W.; Mikati M.A. (SAN DIEGO, 2010)
Prevalence and predictors of immunization in a health insurance plan in a developing country

Sinno D.D.; Shoaib H.A.; Musharrafieh U.M.; Hamadeh G.N. (HOBOKEN, 2009)
Did a ban on diesel-fuel reduce emergency respiratory admissions for children?

El-Zein A.; Nuwayhid I.; El-Fadel M.; Mroueh S. (AMSTERDAM, 2007)
Spectrum of mutations in Lebanese patients with phenylalanine hydroxylase deficiency

Karam P.E.; Alhamra R.S.; Nemer G.; Usta J. (AMSTERDAM, 2013)
HbA1c diagnostic categories and β-cell function relative to insulin sensitivity in overweight-obese adolescents

Sjaarda L.A.; Michaliszyn S.F.; Lee S.; Tfayli H.; Bacha F.; Farchoukh L.; Arslanian S.A. (ALEXANDRIA, 2012)
Spiny follicular hyperkeratotic papules on the face

Ghosn S.; Abboud M.; Kurban M.; Abbas O. (CHICAGO, 2013)
A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome

Chou J.; Hanna-Wakim R.; Tirosh I.; Kane J.; Fraulino D.; Lee Y.N.; Ghanem S.; Mahfouz I.; Megarbane A.; Lefranc G.; Inati A.; Dbaibo G.; Giliani S.; Notarangelo L.D.; Geha R.S.; Massaad M.J. (NEW YORK, 2012)

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