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Developmental Medicine and Child Neurology
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January 1, 1990
Communication and oral-motor function in Rett syndrome
S Budden, M Meek, C Henighan
Neuropediatrics
|
April 1, 1995
Abnormal expression of microtubule-associated protein 2 (MAP-2) in neocortex in Rett syndrome
W E Kaufmann, S Naidu, S Budden
American Journal of Medical Genetics
|
July 1, 1983
Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations
J H DiLiberti, R G Weleber, S Budden
The Journal of Pediatrics
|
July 1, 1993
Dominantly inherited megalencephaly, muscle weakness, and myoliposis: a carnitine-deficient myopathy within the spectrum of the Ruvalcaba-Myhre-Smith syndrome
B R Powell, S S Budden, N R Buist
Brain & Development
|
January 1, 1990
Cerebrospinal fluid studies in the Rett syndrome: biogenic amines and beta-endorphins
S S Budden, E C Myer, I J Butler
Brain & Development
|
September 27, 2005
Clinical profile of a male with Rett syndrome
Sarojini S Budden, Heather C Dorsey, Robert D Steiner
Developmental Medicine and Child Neurology
|
November 1, 1993
Women with cerebral palsy: obstetric experience and neonatal outcome
R Winch, L Bengtson, J McLaughlin, et al.
Neuropediatrics
|
June 1, 1997
Is Rett syndrome caused by a triplet repeat expansion?
S Hofferbert, N C Schanen, S S Budden, et al.
American Journal of Medical Genetics
|
December 1, 1987
Is Angelman syndrome an alternate result of del(15)(q11q13)?
R E Magenis, M G Brown, D A Lacy, et al.
The Journal of Pediatrics
|
January 1, 1986
Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children
S S Budden, N G Kennaway, N R Buist, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Developmental Medicine and Child Neurology
|
January 1, 1990
Communication and oral-motor function in Rett syndrome
S Budden, M Meek, C Henighan
Neuropediatrics
|
April 1, 1995
Abnormal expression of microtubule-associated protein 2 (MAP-2) in neocortex in Rett syndrome
W E Kaufmann, S Naidu, S Budden
American Journal of Medical Genetics
|
July 1, 1983
Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations
J H DiLiberti, R G Weleber, S Budden
The Journal of Pediatrics
|
July 1, 1993
Dominantly inherited megalencephaly, muscle weakness, and myoliposis: a carnitine-deficient myopathy within the spectrum of the Ruvalcaba-Myhre-Smith syndrome
B R Powell, S S Budden, N R Buist
Brain & Development
|
January 1, 1990
Cerebrospinal fluid studies in the Rett syndrome: biogenic amines and beta-endorphins
S S Budden, E C Myer, I J Butler
Brain & Development
|
September 27, 2005
Clinical profile of a male with Rett syndrome
Sarojini S Budden, Heather C Dorsey, Robert D Steiner
Developmental Medicine and Child Neurology
|
November 1, 1993
Women with cerebral palsy: obstetric experience and neonatal outcome
R Winch, L Bengtson, J McLaughlin, et al.
Neuropediatrics
|
June 1, 1997
Is Rett syndrome caused by a triplet repeat expansion?
S Hofferbert, N C Schanen, S S Budden, et al.
American Journal of Medical Genetics
|
December 1, 1987
Is Angelman syndrome an alternate result of del(15)(q11q13)?
R E Magenis, M G Brown, D A Lacy, et al.
The Journal of Pediatrics
|
January 1, 1986
Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children
S S Budden, N G Kennaway, N R Buist, et al.
Page
of 3