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Refinado por: tipo de recurso: Reports remover
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1
Breath-holding spell or epileptic seizure? A description of three girls with epileptic seizures triggered by anoxia
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Report
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Breath-holding spell or epileptic seizure? A description of three girls with epileptic seizures triggered by anoxia

Soto-Insuga, V ; Oses, M ; Castaño-De la Mota, C ; Martínez-Bermejo, A ; Giráldez, B G ; Losada-Del Pozo, R ; Rodrigo-Moreno, M ; Martínez-Cayuelas, E ; Diaz-Gómez, E ; Serratosa, J M

Revista de neurologia, 2020, Vol.71 (8), p.313-314

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2
Dietary management of maternal phenylketonuria with glycomacropeptide and amino acids supplements: A case report
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Dietary management of maternal phenylketonuria with glycomacropeptide and amino acids supplements: A case report

Pinto, A ; Almeida, M F ; Cunha, A ; Carmona, C ; Rocha, S ; Guimas, A ; Ribeiro, R ; Mota, C R ; Martins, E ; MacDonald, A ; Rocha, J C

Molecular genetics and metabolism reports, 2017, Vol.13, p.105-110

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3
Polysubstance use in a Brazilian national sample: Correlates of co-use of alcohol and prescription drugs
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Polysubstance use in a Brazilian national sample: Correlates of co-use of alcohol and prescription drugs

Krawczyk, Noa ; da Mota, Jurema C. ; Coutinho, Carolina ; Bertoni, Neilane ; de Vasconcellos, Mauricio T.L. ; Silva, Pedro L. Nascimento ; De Boni, Raquel B. ; Cerdá, Magdalena ; Bastos, Francisco Inácio

Substance Abuse, 2022, Vol.43 (1), p.520-526

Taylor & Francis

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4
Cerebral vasculitis in Henoch-Schönlein purpura
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Cerebral vasculitis in Henoch-Schönlein purpura

Gonçalves, C ; Ferreira, G ; Mota, C ; Vilarinho, A

Anales de pediatria (Barcelona, Spain : 2003), 2004, Vol.60 (2), p.188-189

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5
Haemolytic uraemic syndrome, cardiomyopathy, cutaneous vasculopathy and anti-phospholipid activity
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Haemolytic uraemic syndrome, cardiomyopathy, cutaneous vasculopathy and anti-phospholipid activity

do Sameiro Faria, M ; Mota, C ; Barbot, J ; Alvares, S ; Jardim, H ; Vilarinho, A ; Pereira, E

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2000, Vol.15 (11), p.1891-1892

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6
Asymptomatic autosomal dominant hypoparathyroidism in six family members of a symptomatic infant
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Asymptomatic autosomal dominant hypoparathyroidism in six family members of a symptomatic infant

Martins, L ; Biscaia, J ; da Mota, H C

The Journal of pediatrics, 1985, Vol.106 (1), p.167-168

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7
Association of dietary lactose and calciuria
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Association of dietary lactose and calciuria

Brandão, A N ; Gonçalves, I ; Cruz, A S ; Mota, H C

Journal of pediatric gastroenterology and nutrition, 1994, Vol.18 (1), p.115-116

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8
Eosinophilic meningoencephalitis due to Toxocara canis
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Eosinophilic meningoencephalitis due to Toxocara canis

Mimoso, M G ; Pereira, M C ; Estevão, M H ; Barroso, A A ; Mota, H C

European journal of pediatrics, 1993, Vol.152 (9), p.783-784

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9
Arthrogryposis multiplex congenita with renal and hepatic abnormalities
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Arthrogryposis multiplex congenita with renal and hepatic abnormalities

Saraiva, J M ; Lemos, C ; Gonçalves, I ; Mota, H C ; Carneiro, F

American journal of medical genetics, 1992, Vol.42 (1), p.140-140

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