Multiple pterygium syndrome: a relatively common disorder among Arabs

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A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13.

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Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene.

Molecular genetics and metabolism·2004

The effect of Vigabatrin, Lamotrigine and Gabapentin on the fertility, weights, sex hormones and biochemical profiles of male rats.

Neuro endocrinology letters·2004

Risk of seizure recurrence after a first unprovoked seizure: a prospective study among Jordanian children.

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BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

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Pan-ethnic preconception screening: evidence from a large-scale programme in a genetically diverse population.

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Knowledge of emerging hypertension challenges among tribal populations in India: An analytical study among medical and allied health professionals.

Journal of family medicine and primary care·2026

Determinants of hypertension medication adherence among older adults in a resource-limited peri-urban setting, Ghana.

Frontiers in public health·2026

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Journal of clinical medicine·2026

Traditional Antipyretic Medicinal Plants Used in Yasothon Province, Northeastern Thailand.

Plants (Basel, Switzerland)·2026

'Some Gave It to Cow, Others to Woman' - Traditional Knowledge and Use of Tuberous Orchids in Hungarian Communities in the Eastern Carpathians (Romania).

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Multiple pterygium syndrome: a relatively common disorder among Arabs

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Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs.

The efficacy and side effects of topiramate on refractory epilepsy in infants and young children: a multi-center clinical trial.

A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13.

Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene.

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Multiple pterygium syndrome: a relatively common disorder among Arabs

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