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Brain & Development
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December 12, 2001
R133C and R168X mutations in Japanese Rett syndrome patients: a caution for misdiagnosis
K Amano, Y Nomura, M Segawa, et al.
Brain & Development
|
December 12, 2001
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases
Y B Yurov, V M Vostrikov, S G Vorsanova, et al.
Brain & Development
|
December 12, 2001
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome
Y B Yurov, S G Vorsanova, A D Kolotii, et al.
Brain & Development
|
December 12, 2001
A 77-year-old woman and a preserved speech variant among the Danish Rett patients with mutations in MECP2
J B Nielsen, K Ravn, M Schwartz
Brain & Development
|
December 12, 2001
Proceedings of the World Congress on Rett Syndrome 2000: Clinico-molecular biological correlation. Karuizawa, Japan. July 24-27, 2000
Brain & Development
|
May 17, 2002
The C677T mutation in the methylenetetrahydrofolate reductase gene contributes to hyperhomocysteinemia in patients taking anticonvulsants
Hiroaki Ono, Akiko Sakamoto, Nobuyuki Mizoguchi, et al.
Brain & Development
|
May 17, 2002
Multimodality functional imaging evaluation in a patient with Rasmussen's encephalitis
Hideaki Ishibashi, Panagiotis G Simos, James W Wheless, et al.
Brain & Development
|
July 27, 2002
Evoked potentials in children with Wilson's disease
Meral Topcu, Mehmet Akif Topcuoglu, Gulsen Kose, et al.
Brain & Development
|
July 27, 2002
Autism, macrocrania and epilepsy: how are they linked?
Antonia Parmeggiani, Annio Posar, Paola Giovanardi-Rossi, et al.
Brain & Development
|
April 27, 2001
Bibliography of congenital muscular dystrophies--cobblestone lissencephalies: series III (1999)
Y Fukuyama
Page
of 516
Search research articles
Search
Showing results (41-50 of 5,159) with videos related to
Sort By:
Page
of 516
Brain & Development
|
December 12, 2001
R133C and R168X mutations in Japanese Rett syndrome patients: a caution for misdiagnosis
K Amano, Y Nomura, M Segawa, et al.
Brain & Development
|
December 12, 2001
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases
Y B Yurov, V M Vostrikov, S G Vorsanova, et al.
Brain & Development
|
December 12, 2001
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome
Y B Yurov, S G Vorsanova, A D Kolotii, et al.
Brain & Development
|
December 12, 2001
A 77-year-old woman and a preserved speech variant among the Danish Rett patients with mutations in MECP2
J B Nielsen, K Ravn, M Schwartz
Brain & Development
|
December 12, 2001
Proceedings of the World Congress on Rett Syndrome 2000: Clinico-molecular biological correlation. Karuizawa, Japan. July 24-27, 2000
Brain & Development
|
May 17, 2002
The C677T mutation in the methylenetetrahydrofolate reductase gene contributes to hyperhomocysteinemia in patients taking anticonvulsants
Hiroaki Ono, Akiko Sakamoto, Nobuyuki Mizoguchi, et al.
Brain & Development
|
May 17, 2002
Multimodality functional imaging evaluation in a patient with Rasmussen's encephalitis
Hideaki Ishibashi, Panagiotis G Simos, James W Wheless, et al.
Brain & Development
|
July 27, 2002
Evoked potentials in children with Wilson's disease
Meral Topcu, Mehmet Akif Topcuoglu, Gulsen Kose, et al.
Brain & Development
|
July 27, 2002
Autism, macrocrania and epilepsy: how are they linked?
Antonia Parmeggiani, Annio Posar, Paola Giovanardi-Rossi, et al.
Brain & Development
|
April 27, 2001
Bibliography of congenital muscular dystrophies--cobblestone lissencephalies: series III (1999)
Y Fukuyama
Page
of 516