Mitochondrial depletion syndrome type 3: the Lebanese variant
Majdalani, Marianne, Yazbeck, Nadine, El Harake, Lamis, Samaha, Jinane, Karam, Pascale E
Published in Frontiers in genetics (29.06.2023)
Published in Frontiers in genetics (29.06.2023)
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Journal Article
Genetic literacy among primary care physicians in a resource-constrained setting
Karam, Pascale E, Hamad, Lina, Elsherif, Mohamed, Kreidieh, Khalil, Nakouzi, Ghunwa, El Asmar, Khalil, Kabakian-Khasholian, Tamar, Curi, Dany Assaf, Yazbek, Soha N
Published in BMC medical education (13.02.2024)
Published in BMC medical education (13.02.2024)
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Journal Article
Kidney and Metabolic Phenotypes in Glycogen Storage Disease Type-I Patients
Aoun, Bilal, Sanjad, Sami, Degheili, Jad A., Barhoumi, Abir, Bassyouni, Amina, Karam, Pascale E.
Published in Frontiers in pediatrics (11.09.2020)
Published in Frontiers in pediatrics (11.09.2020)
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Journal Article
Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: A twelve-year experience
Karam, Pascale E., Habbal, Mohammad-Zuheir, Mikati, Mohamad A., Zaatari, Ghazi E., Cortas, Najwa K., Daher, Rose T.
Published in Clinical biochemistry (01.12.2013)
Published in Clinical biochemistry (01.12.2013)
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Journal Article
Pamidronate Rescue Therapy for Hypercalcemia in a Child With Williams Syndrome
Sanjad, Sami A, Aoun, Bilal, Yammine, Halim, Bassyouni, Amina, Karam, Pascale E
Published in Frontiers in endocrinology (Lausanne) (14.05.2018)
Published in Frontiers in endocrinology (Lausanne) (14.05.2018)
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Journal Article
Hyperornithinemia-hyperammonemia-homocitrullinuria: a rare neurometabolic disorder in two siblings
Rizkallah, Diane, Daher, Rose T., Haddad, Laith, Karam, Pascale E.
Published in Metabolic brain disease (01.06.2024)
Published in Metabolic brain disease (01.06.2024)
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Journal Article
Comb-like EEG pattern in maple syrup urine disease: A case report
Jaafar, Fatima, Haddad, Laith, Habanjar, Dima, Charafeddine, Lama, Yunis, Khalid, Karam, Pascale E., Obeid, Makram
Published in Seizure (London, England) (01.04.2021)
Published in Seizure (London, England) (01.04.2021)
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Journal Article
Outcome of Nonketotic Hyperglycinemia in Lebanon: 14-Year Retrospective Review
Shbarou, Rolla M, Boustany, Rose Mary, Daher, Rose T, Pakdel, Parisa, Noureddine, Abir, Karam, Pascale E
Published in Neuropediatrics (01.08.2019)
Published in Neuropediatrics (01.08.2019)
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Journal Article
Treatable Genetic Metabolic Epilepsies
Assi, Lama, Saklawi, Youssef, Karam, Pascale E., Obeid, Makram
Published in Current treatment options in neurology (01.09.2017)
Published in Current treatment options in neurology (01.09.2017)
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Journal Article
Spectrum of mutations in Lebanese patients with phenylalanine hydroxylase deficiency
Karam, Pascale E., Alhamra, Rasha Shahabeddeen, Nemer, Georges, Usta, Julnar
Published in Gene (15.02.2013)
Published in Gene (15.02.2013)
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Journal Article
Two new familial severe infantile spasm syndromes in males
Karam, Pascale E, Farra, Chantal, Shamseddine, Alhan, Mikati, Mohamad A
Published in Epilepsy & behavior (01.04.2009)
Published in Epilepsy & behavior (01.04.2009)
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Journal Article
Cost-benefit analysis: newborn screening for inborn errors of metabolism in Lebanon
Khneisser, I, Adib, S, Assaad, S, Megarbane, A, Karam, P
Published in Journal of medical screening (01.12.2015)
Published in Journal of medical screening (01.12.2015)
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Journal Article