Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria von Dixon-Salazar, Tracy, Silhavy, Jennifer L., Marsh, Sarah E., Louie, Carrie M., Scott, Lesley C., Gururaj, Aithala, Al-Gazali, Lihadh, Al-Tawari, Asma A., Kayserili, Hulya, Sztriha, László, Gleeson, Joseph G.

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Distinguishing the four genetic causes of jouberts syndrome-related disorders von Valente, Enza Maria, Marsh, Sarah E., Castori, Marco, Dixon-Salazar, Tracy, Bertini, Enrico, Al-Gazali, Lihadh, Messer, Jean, Barbot, Clara, Woods, C. Geoffrey, Boltshauser, Eugen, Al-Tawari, Asma A., Salpietro, Carmelo D., Kayserili, Hulya, Sztriha, László, Gribaa, Moez, Koenig, Michel, Dallapiccola, Bruno, Gleeson, Joseph G.

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Ethylmalonic encephalopathy—report of two cases von Heberle, Lada Cindro, Al Tawari, Asma A., Ramadan, Dina G., Ibrahim, Jamila K.

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An early onset form of methylenetetrahydrofolate reductase deficiency: a report of a family from Kuwait von Al Tawari, Asma A, Ramadan, Dina G, Neubauer, David, Heberle, Lada Cindro, Al Awadi, Fatema

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An early onset form of methylenetetrahydrofolate reductase deficiency: a report of a family from Kuwait von AL TAWARI, Asma A, RAMADAN, Dina G, NEUBAUER, David, LADA CINDRO HEBERLE, FATEMA AL AWADI

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What syndrome is this? Autosomal recessive type II cutis laxa von Nanda, Arti, Lionel, Jesuraj, Al-Tawari, Asma A, Anim, Jehoram Tei

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Brain MRI features of merosin-negative congenital muscular dystrophy von Ibrahim Abdulla, JK, Vattoth, S, Al Tawari, AA, Pandey, T, Abubacker, S

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