Ultrastructure of heart muscle in generalized gangliosidosis GM1

GW240925 and GW250207: Astrophysical Calibration of Gravitational Wave Detectors.

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Black Hole Spectroscopy and Tests of General Relativity with GW250114.

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GW250114: Testing Hawking's Area Law and the Kerr Nature of Black Holes.

Physical review letters·2025

Erratum: Centrality-Dependent Modification of Jet-Production Rates in Deuteron-Gold Collisions at sqrt[s_{NN}]=200 GeV [Phys. Rev. Lett. 116, 122301 (2016)].

Physical review letters·2025

Erratum: Evolution of π^{0} Suppression in Au+Au Collisions from sqrt[s_{NN}]=39 to 200 GeV [Phys. Rev. Lett. 109, 152301 (2012)].

Physical review letters·2020

Beam Energy and Centrality Dependence of Direct-Photon Emission from Ultrarelativistic Heavy-Ion Collisions.

Physical review letters·2019

Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

Zeitschrift fur Kinderheilkunde·1975

[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

[Incidence of malignant tumors in childhood (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

[Differential diagnosis and follow-up studies in sucklings and infants with continuous cholestasis (author's transl)].

Zeitschrift fur Kinderheilkunde·1975

Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

Zeitschrift fur Kinderheilkunde·1975

A rare type of low birthweight dwarfism: the Dubowitz syndrome.

Zeitschrift fur Kinderheilkunde·1975

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

Prenatal diagnosis·2026

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

Experimental biology and medicine (Maywood, N.J.)·2026

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

medRxiv : the preprint server for health sciences·2026

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Balkan medical journal·2026

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Molecular genetics and genomics : MGG·2026

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Ultrastructure of heart muscle in generalized gangliosidosis GM1

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GW240925 and GW250207: Astrophysical Calibration of Gravitational Wave Detectors.

Black Hole Spectroscopy and Tests of General Relativity with GW250114.

GW250114: Testing Hawking's Area Law and the Kerr Nature of Black Holes.

Erratum: Centrality-Dependent Modification of Jet-Production Rates in Deuteron-Gold Collisions at sqrt[s_{NN}]=200 GeV [Phys. Rev. Lett. 116, 122301 (2016)].

Erratum: Evolution of π^{0} Suppression in Au+Au Collisions from sqrt[s_{NN}]=39 to 200 GeV [Phys. Rev. Lett. 109, 152301 (2012)].

Beam Energy and Centrality Dependence of Direct-Photon Emission from Ultrarelativistic Heavy-Ion Collisions.

Ferrous and hemoglobin-59Fe absorption from supplemented cow milk in infants with normal and depleted iron stores.

[The syndrome of inappropriate secretion of antidiuretic hormone and the urinary excretion of aldosterone (author's transl)].

[Incidence of malignant tumors in childhood (author's transl)].

[Differential diagnosis and follow-up studies in sucklings and infants with continuous cholestasis (author's transl)].

Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father).

A rare type of low birthweight dwarfism: the Dubowitz syndrome.

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

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Ultrastructure of heart muscle in generalized gangliosidosis GM1

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