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Carrier frequency of two BBS2 mutations in the Ashkenazi population.

Clinical genetics·2013

Preimplantation genetic diagnosis for BRCA1/2--a novel clinical experience.

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Glutathione-S-transferase M1, T1 and P1 polymorphisms, and breast cancer risk, in BRCA1/2 mutation carriers.

British journal of cancer·2008

Bulimia nervosa and substance use disorder: similarities and differences.

Eating disorders·2008

Increased severity over generations of Charcot-Marie-Tooth disease type 1A.

Journal of neurology·2008

[The Relationship between Physical Activity, Growth, Diagnosis, and Treatment in Children with Attention-Deficit/Hyperactivity Disorder].

Harefuah·2026

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Harefuah·2026

[TAVI Program in Centers without an On-Site Cardiac Surgical Department: Outcomes and Feasibility].

Harefuah·2026

[Methadone vs Fentanyl Patch for Prevention of Agitation in Intensive Care Patients: A Before-After Intervention Study].

Harefuah·2026

[Drug Allergies in Elderly Patients: The Outcomes of Allergic Evaluation and Long-Term Follow-up].

Harefuah·2026

[Medical Management Alone in Symptomatic Free-Floating Thrombus of the Carotid Artery].

Harefuah·2026

SLC52A3-Related Riboflavin Transporter Deficiency in Two Saudi Siblings: A Case Report.

Cureus·2026

Equidistance between primary sensory-motor landmarks shapes functional specialisation in the human brain.

The Journal of neuroscience : the official journal of the Society for Neuroscience·2026

Brachydactyly Type A1 Caused by an IHH Variant in a Patient with Disproportionate Short Stature: A Case Report.

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Lipodystrophy in Central Asia: A Regional Literature Review with a Case Series of Congenital and Acquired Generalized Lipodystrophy.

Metabolites·2026

Sex Steroid Hormone Signaling Tunes Metabolic and Neuronal Programs in Human Cortical Development.

Research square·2026

Single-cell transcriptomic and epigenomic analysis reveals X-linked sex differences in aging mouse hypothalamus.

bioRxiv : the preprint server for biology·2026

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[Diagnostic and genetic aspects of congenital radial ray deficiency]

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Acute Monoblastic Leukemia with t(9;11) in a Patient Receiving Chemotherapy for Ovarian Cancer: Secondary Leukemia or Fortuitous Association of Two Neoplasias?

Carrier frequency of two BBS2 mutations in the Ashkenazi population.

Preimplantation genetic diagnosis for BRCA1/2--a novel clinical experience.

Glutathione-S-transferase M1, T1 and P1 polymorphisms, and breast cancer risk, in BRCA1/2 mutation carriers.

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