Results 201 to 210 of about 125,718 (243)
Some of the next articles are maybe not open access.
Proceedings of the Fifth International Conference on Security of Information and Networks, 2012
As the password based authentication systems are not able to meet the performance because they can be stolen, forgotten, cracked, sniffed and tampered with. Lateral thinking to this problem evolved the use of biometrics to authenticate the person uniquely.
Priyanka Loya, Alwyn Roshan Pais
openaire +2 more sources
As the password based authentication systems are not able to meet the performance because they can be stolen, forgotten, cracked, sniffed and tampered with. Lateral thinking to this problem evolved the use of biometrics to authenticate the person uniquely.
Priyanka Loya, Alwyn Roshan Pais
openaire +2 more sources
Archives of Pediatrics & Adolescent Medicine, 1978
We present the sixth reported case of the Coffin-Siris syndrome. This disorder is characterized by the absence of the nails of the fifth fingers and toes, severe mental and developmental retardation, and postnatal growth deficiency. Feeding and respiratory problems are prominent features.
W W, Tunnessen +2 more
openaire +4 more sources
We present the sixth reported case of the Coffin-Siris syndrome. This disorder is characterized by the absence of the nails of the fifth fingers and toes, severe mental and developmental retardation, and postnatal growth deficiency. Feeding and respiratory problems are prominent features.
W W, Tunnessen +2 more
openaire +4 more sources
Archives of Neurology, 1985
We studied the neuropathologic features of a patient with Coffin-Siris syndrome. Two previously reported cases showed Dandy-Walker (D-W) malformations. In the present case there was no evidence of D-W malformation; instead there were hindbrain abnormalities of inferior and medial accessory olives, large arcuate nuclei, heterotopic olivary nuclei, and ...
W A, DeBassio, T L, Kemper, J E, Knoefel
openaire +2 more sources
We studied the neuropathologic features of a patient with Coffin-Siris syndrome. Two previously reported cases showed Dandy-Walker (D-W) malformations. In the present case there was no evidence of D-W malformation; instead there were hindbrain abnormalities of inferior and medial accessory olives, large arcuate nuclei, heterotopic olivary nuclei, and ...
W A, DeBassio, T L, Kemper, J E, Knoefel
openaire +2 more sources
Acta Paediatrica, 1979
Abstract. A 14‐month‐old female with the Coffin‐Siris syndrome is described. Typical features included underweight at birth, growth retardation, microcephaly, profound mental retardation, severe hypotonia with lax joints, feeding difficulties and frequent respiratory tract infections; sparce scalp hair, small nose, epicanthic folds, a prominent ...
openaire +3 more sources
Abstract. A 14‐month‐old female with the Coffin‐Siris syndrome is described. Typical features included underweight at birth, growth retardation, microcephaly, profound mental retardation, severe hypotonia with lax joints, feeding difficulties and frequent respiratory tract infections; sparce scalp hair, small nose, epicanthic folds, a prominent ...
openaire +3 more sources
2005
Moscati Castelnuovo Luisa,Lambrugo Claudia. SIRI . In: Bibliografia topografica della colonizzazione greca in Italia e nelle Isole Tirreniche, n°19, 2005. Siti : Siracusa - Surbo. pp. 387-424.
C. Lambrugo, L. M. Castelnuovo
openaire +2 more sources
Moscati Castelnuovo Luisa,Lambrugo Claudia. SIRI . In: Bibliografia topografica della colonizzazione greca in Italia e nelle Isole Tirreniche, n°19, 2005. Siti : Siracusa - Surbo. pp. 387-424.
C. Lambrugo, L. M. Castelnuovo
openaire +2 more sources
Archives of Pediatrics & Adolescent Medicine, 1985
Sir .—One additional feature, aplasia of the uterus, eventually may be added to the syndrome that we have already described. 1 We are still in contact with one patient who has this syndrome: she is listed as patient 3 in our original article, and as patient 6 in a later communication by Carey and Hall. 2 When the patient reached the age of 21 years and
G S, Coffin, E, Siris
openaire +2 more sources
Sir .—One additional feature, aplasia of the uterus, eventually may be added to the syndrome that we have already described. 1 We are still in contact with one patient who has this syndrome: she is listed as patient 3 in our original article, and as patient 6 in a later communication by Carey and Hall. 2 When the patient reached the age of 21 years and
G S, Coffin, E, Siris
openaire +2 more sources
Siris rystelser:om Siri Hustvedts "Kvinden der rystede"
2011Om hysteri mellem biologi, neurologi og psykologi. Psykosomatik og identitet.
openaire +2 more sources
Archives of Pediatrics & Adolescent Medicine, 1978
Sir .—We were interested in the report in theJournal(132:393-395, 1978) by Tunnessen et al on Coffin-Siris syndrome. During the past two years we have seen three cases suggestive of this condition. Report of Cases .—A 4-year-old boy was severely microcephalic but lacked any nail abnormalities.
openaire +1 more source
Sir .—We were interested in the report in theJournal(132:393-395, 1978) by Tunnessen et al on Coffin-Siris syndrome. During the past two years we have seen three cases suggestive of this condition. Report of Cases .—A 4-year-old boy was severely microcephalic but lacked any nail abnormalities.
openaire +1 more source